Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1247809.RA86uLtY3rAABY5FH3uaJWNqh1mIvE3H_q9RZAWIc5GTI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1247809.RA86uLtY3rAABY5FH3uaJWNqh1mIvE3H_q9RZAWIc5GTI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1247809.RA86uLtY3rAABY5FH3uaJWNqh1mIvE3H_q9RZAWIc5GTI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1247809.RA86uLtY3rAABY5FH3uaJWNqh1mIvE3H_q9RZAWIc5GTI130_provenance.
- NP1247809.RA86uLtY3rAABY5FH3uaJWNqh1mIvE3H_q9RZAWIc5GTI130_assertion description "[The common phenotype of nuclear receptor superfamily 5, group A, member 1 (NR5A1) gene mutations in 46,XY is gonadal dysgenesis without adrenal deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1247809.RA86uLtY3rAABY5FH3uaJWNqh1mIvE3H_q9RZAWIc5GTI130_provenance.
- NP1247809.RA86uLtY3rAABY5FH3uaJWNqh1mIvE3H_q9RZAWIc5GTI130_assertion evidence source_evidence_literature NP1247809.RA86uLtY3rAABY5FH3uaJWNqh1mIvE3H_q9RZAWIc5GTI130_provenance.
- NP1247809.RA86uLtY3rAABY5FH3uaJWNqh1mIvE3H_q9RZAWIc5GTI130_assertion SIO_000772 25502990 NP1247809.RA86uLtY3rAABY5FH3uaJWNqh1mIvE3H_q9RZAWIc5GTI130_provenance.
- NP1247809.RA86uLtY3rAABY5FH3uaJWNqh1mIvE3H_q9RZAWIc5GTI130_assertion wasDerivedFrom befree-2016 NP1247809.RA86uLtY3rAABY5FH3uaJWNqh1mIvE3H_q9RZAWIc5GTI130_provenance.
- NP1247809.RA86uLtY3rAABY5FH3uaJWNqh1mIvE3H_q9RZAWIc5GTI130_assertion wasGeneratedBy ECO_0000203 NP1247809.RA86uLtY3rAABY5FH3uaJWNqh1mIvE3H_q9RZAWIc5GTI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1247809.RA86uLtY3rAABY5FH3uaJWNqh1mIvE3H_q9RZAWIc5GTI130_provenance.