Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP535169.RAoT_kCR2x94R2I_cCXsXsVgr1ASgr6hfjBDNEfxK9eYM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP535169.RAoT_kCR2x94R2I_cCXsXsVgr1ASgr6hfjBDNEfxK9eYM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP535169.RAoT_kCR2x94R2I_cCXsXsVgr1ASgr6hfjBDNEfxK9eYM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP535169.RAoT_kCR2x94R2I_cCXsXsVgr1ASgr6hfjBDNEfxK9eYM130_provenance.
- NP535169.RAoT_kCR2x94R2I_cCXsXsVgr1ASgr6hfjBDNEfxK9eYM130_assertion wasGeneratedBy ECO_0000203 NP535169.RAoT_kCR2x94R2I_cCXsXsVgr1ASgr6hfjBDNEfxK9eYM130_provenance.
- NP535169.RAoT_kCR2x94R2I_cCXsXsVgr1ASgr6hfjBDNEfxK9eYM130_assertion wasDerivedFrom befree-20140225 NP535169.RAoT_kCR2x94R2I_cCXsXsVgr1ASgr6hfjBDNEfxK9eYM130_provenance.
- NP535169.RAoT_kCR2x94R2I_cCXsXsVgr1ASgr6hfjBDNEfxK9eYM130_assertion SIO_000772 19785597 NP535169.RAoT_kCR2x94R2I_cCXsXsVgr1ASgr6hfjBDNEfxK9eYM130_provenance.
- NP535169.RAoT_kCR2x94R2I_cCXsXsVgr1ASgr6hfjBDNEfxK9eYM130_assertion evidence source_evidence_literature NP535169.RAoT_kCR2x94R2I_cCXsXsVgr1ASgr6hfjBDNEfxK9eYM130_provenance.
- NP535169.RAoT_kCR2x94R2I_cCXsXsVgr1ASgr6hfjBDNEfxK9eYM130_assertion description "[This observation suggests that coinheritance of mutations in KRT16 and FLG may aggravate the PC phenotype and that FLG could serve as a genetic modifier in PC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP535169.RAoT_kCR2x94R2I_cCXsXsVgr1ASgr6hfjBDNEfxK9eYM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP535169.RAoT_kCR2x94R2I_cCXsXsVgr1ASgr6hfjBDNEfxK9eYM130_provenance.