Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP674522.RAfzEwWhUdn6TWlCGYM3oDRjP9xyg2XT7QJ0h2oQm3xmo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP674522.RAfzEwWhUdn6TWlCGYM3oDRjP9xyg2XT7QJ0h2oQm3xmo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP674522.RAfzEwWhUdn6TWlCGYM3oDRjP9xyg2XT7QJ0h2oQm3xmo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP674522.RAfzEwWhUdn6TWlCGYM3oDRjP9xyg2XT7QJ0h2oQm3xmo130_provenance.
- NP674522.RAfzEwWhUdn6TWlCGYM3oDRjP9xyg2XT7QJ0h2oQm3xmo130_assertion description "[Allelic heterogeneity and genetic modifier loci contribute to clinical variation in males with X-linked retinitis pigmentosa due to RPGR mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674522.RAfzEwWhUdn6TWlCGYM3oDRjP9xyg2XT7QJ0h2oQm3xmo130_provenance.
- NP674522.RAfzEwWhUdn6TWlCGYM3oDRjP9xyg2XT7QJ0h2oQm3xmo130_assertion evidence source_evidence_literature NP674522.RAfzEwWhUdn6TWlCGYM3oDRjP9xyg2XT7QJ0h2oQm3xmo130_provenance.
- NP674522.RAfzEwWhUdn6TWlCGYM3oDRjP9xyg2XT7QJ0h2oQm3xmo130_assertion SIO_000772 21857984 NP674522.RAfzEwWhUdn6TWlCGYM3oDRjP9xyg2XT7QJ0h2oQm3xmo130_provenance.
- NP674522.RAfzEwWhUdn6TWlCGYM3oDRjP9xyg2XT7QJ0h2oQm3xmo130_assertion wasDerivedFrom befree-20150227 NP674522.RAfzEwWhUdn6TWlCGYM3oDRjP9xyg2XT7QJ0h2oQm3xmo130_provenance.
- NP674522.RAfzEwWhUdn6TWlCGYM3oDRjP9xyg2XT7QJ0h2oQm3xmo130_assertion wasGeneratedBy ECO_0000203 NP674522.RAfzEwWhUdn6TWlCGYM3oDRjP9xyg2XT7QJ0h2oQm3xmo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP674522.RAfzEwWhUdn6TWlCGYM3oDRjP9xyg2XT7QJ0h2oQm3xmo130_provenance.