reference/13864788

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/13864788

Outgoing Links

Predicate	Object
contentType	Journal Article
endingPage	1327
issn	0002-9297
issueIdentifier	5
pageRange	1318-1327
publicationName	The American Journal of Human Genetics
startingPage	1318
hasFundingAgency	http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_5a0eb2fadabf1dffb4d70280b760adba http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_e423e98d115894f5b30465dcb1113e0c
isSupportedBy	http://rdf.ncbi.nlm.nih.gov/pubchem/grant/MD5_a1130afb513930ecb2d87a6be758625a http://rdf.ncbi.nlm.nih.gov/pubchem/grant/MD5_dfd3e8abeec0c2b5b31e2331bbbabf22
bibliographicCitation	Newbury DF, Bonora E, Lamb JA, Fisher SE, Lai CS, Baird G, Jannoun L, Slonims V, Stott CM, Merricks MJ, Bolton PF, Bailey AJ, Monaco AP; International Molecular Genetic Study of Autism Consortium. FOXP2 is not a major susceptibility gene for autism or specific language impairment. Am J Hum Genet. 2002 May;70(5):1318–27. PMID: 11894222; PMCID: PMC447606.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_262cd0ee9dd0583870051fd72c723e39 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_5b2810cc9c7f1094b673d46fbdd91921 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_c05e5024b74737a55603f8a1d704d9f9 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_e9d07b41f42b2d04f300940668d0eea7 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a54890dd6d00f1ec4c53885b10269361 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_2cefbbdbf0cda37f779334befdcc4f1f http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_ff70e20c9f7e1571b55bf047808f3e00 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_f44737c6396b403ae7c4b489206874ce http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_30129f29369d8e08a599ea67600ee773 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_7fd6a20571f239a92139a4e508e4d81f http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_74f89416ddd38b64f7499ea32bd196c5 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a59697cc99cd65451742b4c179444f7a http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_a218be2034ad26bc213019f424df359c
date	200205
identifier	https://pubmed.ncbi.nlm.nih.gov/11894222 https://doi.org/10.1086/339931 https://pubmed.ncbi.nlm.nih.gov/PMC447606
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	FOXP2 Is Not a Major Susceptibility Gene for Autism or Specific Language Impairment
discusses	http://id.nlm.nih.gov/mesh/M0166232 http://id.nlm.nih.gov/mesh/M0021788 http://id.nlm.nih.gov/mesh/M0018809 http://id.nlm.nih.gov/mesh/M0438847
hasPrimarySubjectTerm	http://id.nlm.nih.gov/mesh/D007806Q000235 http://id.nlm.nih.gov/mesh/D014157 http://id.nlm.nih.gov/mesh/D012097Q000235 http://id.nlm.nih.gov/mesh/D001321Q000235 http://id.nlm.nih.gov/mesh/D020022Q000235
hasSubjectTerm	http://id.nlm.nih.gov/mesh/D005091Q000235 http://id.nlm.nih.gov/mesh/D000595 http://id.nlm.nih.gov/mesh/D018895Q000235 http://id.nlm.nih.gov/mesh/D005820 http://id.nlm.nih.gov/mesh/D051858 http://id.nlm.nih.gov/mesh/D001483 http://id.nlm.nih.gov/mesh/D005260 http://id.nlm.nih.gov/mesh/D004252 http://id.nlm.nih.gov/mesh/D020641Q000235 http://id.nlm.nih.gov/mesh/D000483 http://id.nlm.nih.gov/mesh/D006801 http://id.nlm.nih.gov/mesh/D008297 http://id.nlm.nih.gov/mesh/D008969 http://id.nlm.nih.gov/mesh/D010375 http://id.nlm.nih.gov/mesh/D005787 http://id.nlm.nih.gov/mesh/D007438Q000235
discussesAsDerivedByTextMining	http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID9476 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID6709 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID7000 http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8265 http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_d1900b47fed72c36f2ed3b2e61cd69af

Incoming Links

Predicate	Subject
isDiscussedBy	http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID93986

Total number of triples: 66.