reference/25122592

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/25122592

Outgoing Links

Predicate	Object
contentType	Case Reports\|Journal Article\|Research Support, Non-U.S. Gov't
endingPage	764
issn	0002-9297
issueIdentifier	3
pageRange	759-764
publicationName	The American Journal of Human Genetics
startingPage	759
hasFundingAgency	http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_f4b0b5cd5a2336c0dab358b1a941e55b
isSupportedBy	http://rdf.ncbi.nlm.nih.gov/pubchem/grant/MD5_e5a4c8f0672226d2dee92918c0435ab0 http://rdf.ncbi.nlm.nih.gov/pubchem/grant/MD5_8966341727e10dc983a1c607c55d91d1
bibliographicCitation	Guida S, Trettel F, Pagnutti S, Mantuano E, Tottene A, Veneziano L, Fellin T, Spadaro M, Stauderman KA, Williams ME, Volsen S, Ophoff RA, Frants RR, Jodice C, Frontali M, Pietrobon D. Complete Loss of P/Q Calcium Channel Activity Caused by a CACNA1A Missense Mutation Carried by Patients with Episodic Ataxia Type 2. The American Journal of Human Genetics. 2001 Mar;68(3):759–64. doi: 10.1086/318804.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_486339bcd97f092f136e458670fb1c62 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_fe73e26309a78383e66fe3fed6a53f85 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_d9e714e378964983e36d572a82bd8314 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-1549-5005 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_c2c62e069a0acefc7d3ddd6a9ab76143 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_65fa2a113b73b399c1062e41ef8819be http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_2c1626aa81ba0be586c590d3c1d59110 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_91ad96a92aad745a61c1e73d9c54f000 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-7983-2955 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_ca992bb959d7a9acda486bf7feb79b72 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_08800282679f09cb86562036c144b5c4 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_65084cee023591a83ffb59fae828195b http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0003-1656-5543 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_3dac9a99ff14df91636a32039e71b5a0 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_49da13374072c16f4e880c36e408094a http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0002-9921-8450 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_67f8d82d2713191b9d8b352d68a7bad0 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a987000251d2e86a229eba549069237a http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_76d1dc26d67fa5a199218bfc84447d2a http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_87ff5321f832e30598c3fbb7d1be5d8c
date	200103
identifier	https://doi.org/10.1086/318804 https://pubmed.ncbi.nlm.nih.gov/PMC1274487 https://pubmed.ncbi.nlm.nih.gov/11179022
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/428 https://portal.issn.org/resource/ISSN/0002-9297
language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Complete Loss of P/Q Calcium Channel Activity Caused by a CACNA1A Missense Mutation Carried by Patients with Episodic Ataxia Type 2
discusses	http://id.nlm.nih.gov/mesh/M0440212 http://id.nlm.nih.gov/mesh/M0023383 http://id.nlm.nih.gov/mesh/M0351591 http://id.nlm.nih.gov/mesh/M0328057 http://id.nlm.nih.gov/mesh/M0328058
hasPrimarySubjectTerm	http://id.nlm.nih.gov/mesh/D002524Q000235 http://id.nlm.nih.gov/mesh/D020125 http://id.nlm.nih.gov/mesh/D015220Q000235 http://id.nlm.nih.gov/mesh/D002888
hasSubjectTerm	http://id.nlm.nih.gov/mesh/D008297 http://id.nlm.nih.gov/mesh/D010375 http://id.nlm.nih.gov/mesh/D008958 http://id.nlm.nih.gov/mesh/D008564Q000502 http://id.nlm.nih.gov/mesh/D002874 http://id.nlm.nih.gov/mesh/D002460 http://id.nlm.nih.gov/mesh/D018408 http://id.nlm.nih.gov/mesh/D017433 http://id.nlm.nih.gov/mesh/D002524Q000145 http://id.nlm.nih.gov/mesh/D016297 http://id.nlm.nih.gov/mesh/D015220Q000502 http://id.nlm.nih.gov/mesh/D014162 http://id.nlm.nih.gov/mesh/D000595 http://id.nlm.nih.gov/mesh/D015220Q000737 http://id.nlm.nih.gov/mesh/D021122 http://id.nlm.nih.gov/mesh/D020907Q000235 http://id.nlm.nih.gov/mesh/D020865Q000235 http://id.nlm.nih.gov/mesh/D008969 http://id.nlm.nih.gov/mesh/D006801 http://id.nlm.nih.gov/mesh/D005260
discussesAsDerivedByTextMining	http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID10615 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6140 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_9ffa6b56d06ddd0c9bc50088955e425b http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID341 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID10552 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5951 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_9eb90d8089507e15a0c653cdd3ce8c18

Incoming Links

Predicate	Subject
isDiscussedBy	http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127654813 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID773 http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128643942

Total number of triples: 80.