Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP823082.RASZz7GHUyi-sZBm4SO6b3088YNA4AxIWK1RRl4RzD10U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP823082.RASZz7GHUyi-sZBm4SO6b3088YNA4AxIWK1RRl4RzD10U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP823082.RASZz7GHUyi-sZBm4SO6b3088YNA4AxIWK1RRl4RzD10U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP823082.RASZz7GHUyi-sZBm4SO6b3088YNA4AxIWK1RRl4RzD10U130_provenance.
- NP823082.RASZz7GHUyi-sZBm4SO6b3088YNA4AxIWK1RRl4RzD10U130_assertion description "[More recently, heterozygous NR5A1 mutations have been identified in a substantial proportion of patients with 46,XY disorders of sex development (46,XY DSD) without adrenal insufficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP823082.RASZz7GHUyi-sZBm4SO6b3088YNA4AxIWK1RRl4RzD10U130_provenance.
- NP823082.RASZz7GHUyi-sZBm4SO6b3088YNA4AxIWK1RRl4RzD10U130_assertion evidence source_evidence_literature NP823082.RASZz7GHUyi-sZBm4SO6b3088YNA4AxIWK1RRl4RzD10U130_provenance.
- NP823082.RASZz7GHUyi-sZBm4SO6b3088YNA4AxIWK1RRl4RzD10U130_assertion SIO_000772 20595937 NP823082.RASZz7GHUyi-sZBm4SO6b3088YNA4AxIWK1RRl4RzD10U130_provenance.
- NP823082.RASZz7GHUyi-sZBm4SO6b3088YNA4AxIWK1RRl4RzD10U130_assertion wasDerivedFrom befree-2016 NP823082.RASZz7GHUyi-sZBm4SO6b3088YNA4AxIWK1RRl4RzD10U130_provenance.
- NP823082.RASZz7GHUyi-sZBm4SO6b3088YNA4AxIWK1RRl4RzD10U130_assertion wasGeneratedBy ECO_0000203 NP823082.RASZz7GHUyi-sZBm4SO6b3088YNA4AxIWK1RRl4RzD10U130_provenance.
- befree-2016 importedOn "2016-02-19" NP823082.RASZz7GHUyi-sZBm4SO6b3088YNA4AxIWK1RRl4RzD10U130_provenance.