| Predicate |
Object |
| contentType |
Journal Article|Research Support, Non-U.S. Gov't |
| issn |
1479-7364 |
| issueIdentifier |
1 |
| pageRange |
41- |
| publicationName |
Human Genomics |
| startingPage |
41 |
| bibliographicCitation |
Chograni M, Alahdal HM, Rejili M. Autosomal recessive congenital cataract is associated with a novel 4-bp splicing deletion mutation in a novel C10orf71 human gene. Hum Genomics. 2023 May 13;17(1):41. PMID: 37179318; PMCID: PMC10182639. |
| creator |
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_913d95b4372457d4f8e0195b45a67c32
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_df339c823c0944bdd369040946fd050e
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_484915f5f290e37951d3802e139eba99 |
| date |
2023-05-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| identifier |
https://pubmed.ncbi.nlm.nih.gov/37179318
https://doi.org/10.1186/s40246-023-00492-6
https://pubmed.ncbi.nlm.nih.gov/PMC10182639 |
| isPartOf |
http://rdf.ncbi.nlm.nih.gov/pubchem/journal/32174
https://portal.issn.org/resource/ISSN/1479-7364 |
| language |
English |
| source |
https://www.crossref.org/
https://pubmed.ncbi.nlm.nih.gov/ |
| title |
Autosomal recessive congenital cataract is associated with a novel 4-bp splicing deletion mutation in a novel C10orf71 human gene |
| discusses |
http://id.nlm.nih.gov/mesh/M0359363 |
| discussesAsDerivedByTextMining |
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8600
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID7725
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/MD5_202eedb37b6fcdbe76faab36ecf61341
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8489
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID8539
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID7191 |