Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP413654.RAZIlJkgkcU6LnRhgvgnWEWNwaWReGstDE0f5vPQWZN2E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP413654.RAZIlJkgkcU6LnRhgvgnWEWNwaWReGstDE0f5vPQWZN2E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP413654.RAZIlJkgkcU6LnRhgvgnWEWNwaWReGstDE0f5vPQWZN2E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP413654.RAZIlJkgkcU6LnRhgvgnWEWNwaWReGstDE0f5vPQWZN2E130_provenance.
- NP413654.RAZIlJkgkcU6LnRhgvgnWEWNwaWReGstDE0f5vPQWZN2E130_assertion description "[SF-1/NR5A1 mutations are frequently found in 46,XY DSD individuals (9%) and manifest with a broad phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP413654.RAZIlJkgkcU6LnRhgvgnWEWNwaWReGstDE0f5vPQWZN2E130_provenance.
- NP413654.RAZIlJkgkcU6LnRhgvgnWEWNwaWReGstDE0f5vPQWZN2E130_assertion evidence source_evidence_literature NP413654.RAZIlJkgkcU6LnRhgvgnWEWNwaWReGstDE0f5vPQWZN2E130_provenance.
- NP413654.RAZIlJkgkcU6LnRhgvgnWEWNwaWReGstDE0f5vPQWZN2E130_assertion SIO_000772 22549935 NP413654.RAZIlJkgkcU6LnRhgvgnWEWNwaWReGstDE0f5vPQWZN2E130_provenance.
- NP413654.RAZIlJkgkcU6LnRhgvgnWEWNwaWReGstDE0f5vPQWZN2E130_assertion wasDerivedFrom befree-20150227 NP413654.RAZIlJkgkcU6LnRhgvgnWEWNwaWReGstDE0f5vPQWZN2E130_provenance.
- NP413654.RAZIlJkgkcU6LnRhgvgnWEWNwaWReGstDE0f5vPQWZN2E130_assertion wasGeneratedBy ECO_0000203 NP413654.RAZIlJkgkcU6LnRhgvgnWEWNwaWReGstDE0f5vPQWZN2E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP413654.RAZIlJkgkcU6LnRhgvgnWEWNwaWReGstDE0f5vPQWZN2E130_provenance.