Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP165194.RAD5RPNg2DO9S4JuhbricAtjwCxOsN-kZ5dlWiPrQ78cg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP165194.RAD5RPNg2DO9S4JuhbricAtjwCxOsN-kZ5dlWiPrQ78cg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP165194.RAD5RPNg2DO9S4JuhbricAtjwCxOsN-kZ5dlWiPrQ78cg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP165194.RAD5RPNg2DO9S4JuhbricAtjwCxOsN-kZ5dlWiPrQ78cg130_provenance.
- NP165194.RAD5RPNg2DO9S4JuhbricAtjwCxOsN-kZ5dlWiPrQ78cg130_assertion description "[Analysis of mutant SRY, SF1 and SOX9 proteins encoded by thirteen separate 46,XY DSD gonadal dysgenesis individuals reveals a reduced ability to activate hTES.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP165194.RAD5RPNg2DO9S4JuhbricAtjwCxOsN-kZ5dlWiPrQ78cg130_provenance.
- NP165194.RAD5RPNg2DO9S4JuhbricAtjwCxOsN-kZ5dlWiPrQ78cg130_assertion evidence source_evidence_literature NP165194.RAD5RPNg2DO9S4JuhbricAtjwCxOsN-kZ5dlWiPrQ78cg130_provenance.
- NP165194.RAD5RPNg2DO9S4JuhbricAtjwCxOsN-kZ5dlWiPrQ78cg130_assertion SIO_000772 21412441 NP165194.RAD5RPNg2DO9S4JuhbricAtjwCxOsN-kZ5dlWiPrQ78cg130_provenance.
- NP165194.RAD5RPNg2DO9S4JuhbricAtjwCxOsN-kZ5dlWiPrQ78cg130_assertion wasDerivedFrom befree-20140225 NP165194.RAD5RPNg2DO9S4JuhbricAtjwCxOsN-kZ5dlWiPrQ78cg130_provenance.
- NP165194.RAD5RPNg2DO9S4JuhbricAtjwCxOsN-kZ5dlWiPrQ78cg130_assertion wasGeneratedBy ECO_0000203 NP165194.RAD5RPNg2DO9S4JuhbricAtjwCxOsN-kZ5dlWiPrQ78cg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP165194.RAD5RPNg2DO9S4JuhbricAtjwCxOsN-kZ5dlWiPrQ78cg130_provenance.