Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP9490.RACUuAoukgg6pIJQBUjXB7FTam9uHn8AfEIcFk4w-u_pY130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP9490.RACUuAoukgg6pIJQBUjXB7FTam9uHn8AfEIcFk4w-u_pY130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP9490.RACUuAoukgg6pIJQBUjXB7FTam9uHn8AfEIcFk4w-u_pY130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP9490.RACUuAoukgg6pIJQBUjXB7FTam9uHn8AfEIcFk4w-u_pY130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP9490.RACUuAoukgg6pIJQBUjXB7FTam9uHn8AfEIcFk4w-u_pY130_provenance.
- NP9490.RACUuAoukgg6pIJQBUjXB7FTam9uHn8AfEIcFk4w-u_pY130_assertion wasGeneratedBy ECO_0000218 NP9490.RACUuAoukgg6pIJQBUjXB7FTam9uHn8AfEIcFk4w-u_pY130_provenance.
- NP9490.RACUuAoukgg6pIJQBUjXB7FTam9uHn8AfEIcFk4w-u_pY130_assertion wasDerivedFrom uniprot-2016 NP9490.RACUuAoukgg6pIJQBUjXB7FTam9uHn8AfEIcFk4w-u_pY130_provenance.
- NP9490.RACUuAoukgg6pIJQBUjXB7FTam9uHn8AfEIcFk4w-u_pY130_assertion SIO_000772 9302173 NP9490.RACUuAoukgg6pIJQBUjXB7FTam9uHn8AfEIcFk4w-u_pY130_provenance.
- NP9490.RACUuAoukgg6pIJQBUjXB7FTam9uHn8AfEIcFk4w-u_pY130_assertion evidence source_evidence_curated NP9490.RACUuAoukgg6pIJQBUjXB7FTam9uHn8AfEIcFk4w-u_pY130_provenance.
- NP9490.RACUuAoukgg6pIJQBUjXB7FTam9uHn8AfEIcFk4w-u_pY130_assertion description "[Androgen receptor point mutations as the underlying molecular defect in 2 patients with androgen insensitivity syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9490.RACUuAoukgg6pIJQBUjXB7FTam9uHn8AfEIcFk4w-u_pY130_provenance.