Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP281681.RA4yhV9bt_OEcVfjKgEkyUYlu605N19XhyTsyq8n5fZM0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP281681.RA4yhV9bt_OEcVfjKgEkyUYlu605N19XhyTsyq8n5fZM0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP281681.RA4yhV9bt_OEcVfjKgEkyUYlu605N19XhyTsyq8n5fZM0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP281681.RA4yhV9bt_OEcVfjKgEkyUYlu605N19XhyTsyq8n5fZM0130_provenance.
- NP281681.RA4yhV9bt_OEcVfjKgEkyUYlu605N19XhyTsyq8n5fZM0130_assertion description "[This result suggests that 46,XY DSD patient phenotypes may be influenced by SRD5A2 polymorphism genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP281681.RA4yhV9bt_OEcVfjKgEkyUYlu605N19XhyTsyq8n5fZM0130_provenance.
- NP281681.RA4yhV9bt_OEcVfjKgEkyUYlu605N19XhyTsyq8n5fZM0130_assertion evidence source_evidence_literature NP281681.RA4yhV9bt_OEcVfjKgEkyUYlu605N19XhyTsyq8n5fZM0130_provenance.
- NP281681.RA4yhV9bt_OEcVfjKgEkyUYlu605N19XhyTsyq8n5fZM0130_assertion SIO_000772 21631525 NP281681.RA4yhV9bt_OEcVfjKgEkyUYlu605N19XhyTsyq8n5fZM0130_provenance.
- NP281681.RA4yhV9bt_OEcVfjKgEkyUYlu605N19XhyTsyq8n5fZM0130_assertion wasDerivedFrom befree-20140225 NP281681.RA4yhV9bt_OEcVfjKgEkyUYlu605N19XhyTsyq8n5fZM0130_provenance.
- NP281681.RA4yhV9bt_OEcVfjKgEkyUYlu605N19XhyTsyq8n5fZM0130_assertion wasGeneratedBy ECO_0000203 NP281681.RA4yhV9bt_OEcVfjKgEkyUYlu605N19XhyTsyq8n5fZM0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP281681.RA4yhV9bt_OEcVfjKgEkyUYlu605N19XhyTsyq8n5fZM0130_provenance.