Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP410493.RAc0X46reNMCtS6WP2IjOOolt7pcFfoTKyAMS7_KtjkUY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP410493.RAc0X46reNMCtS6WP2IjOOolt7pcFfoTKyAMS7_KtjkUY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP410493.RAc0X46reNMCtS6WP2IjOOolt7pcFfoTKyAMS7_KtjkUY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP410493.RAc0X46reNMCtS6WP2IjOOolt7pcFfoTKyAMS7_KtjkUY130_provenance.
- NP410493.RAc0X46reNMCtS6WP2IjOOolt7pcFfoTKyAMS7_KtjkUY130_assertion description "[We identified an inherited brain-specific folate transport defect that is caused by mutations in the folate receptor 1 (FOLR1) gene coding for folate receptor alpha (FRalpha).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP410493.RAc0X46reNMCtS6WP2IjOOolt7pcFfoTKyAMS7_KtjkUY130_provenance.
- NP410493.RAc0X46reNMCtS6WP2IjOOolt7pcFfoTKyAMS7_KtjkUY130_assertion evidence source_evidence_literature NP410493.RAc0X46reNMCtS6WP2IjOOolt7pcFfoTKyAMS7_KtjkUY130_provenance.
- NP410493.RAc0X46reNMCtS6WP2IjOOolt7pcFfoTKyAMS7_KtjkUY130_assertion SIO_000772 19732866 NP410493.RAc0X46reNMCtS6WP2IjOOolt7pcFfoTKyAMS7_KtjkUY130_provenance.
- NP410493.RAc0X46reNMCtS6WP2IjOOolt7pcFfoTKyAMS7_KtjkUY130_assertion wasDerivedFrom befree-20150227 NP410493.RAc0X46reNMCtS6WP2IjOOolt7pcFfoTKyAMS7_KtjkUY130_provenance.
- NP410493.RAc0X46reNMCtS6WP2IjOOolt7pcFfoTKyAMS7_KtjkUY130_assertion wasGeneratedBy ECO_0000203 NP410493.RAc0X46reNMCtS6WP2IjOOolt7pcFfoTKyAMS7_KtjkUY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP410493.RAc0X46reNMCtS6WP2IjOOolt7pcFfoTKyAMS7_KtjkUY130_provenance.