Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP736697.RAB2J9GI8KmRHaEGwiQT1Yq967QqHt35vwXLARoGZ5s6A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP736697.RAB2J9GI8KmRHaEGwiQT1Yq967QqHt35vwXLARoGZ5s6A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP736697.RAB2J9GI8KmRHaEGwiQT1Yq967QqHt35vwXLARoGZ5s6A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP736697.RAB2J9GI8KmRHaEGwiQT1Yq967QqHt35vwXLARoGZ5s6A130_provenance.
- befree-2016 importedOn "2016-02-19" NP736697.RAB2J9GI8KmRHaEGwiQT1Yq967QqHt35vwXLARoGZ5s6A130_provenance.
- NP736697.RAB2J9GI8KmRHaEGwiQT1Yq967QqHt35vwXLARoGZ5s6A130_assertion wasGeneratedBy ECO_0000203 NP736697.RAB2J9GI8KmRHaEGwiQT1Yq967QqHt35vwXLARoGZ5s6A130_provenance.
- NP736697.RAB2J9GI8KmRHaEGwiQT1Yq967QqHt35vwXLARoGZ5s6A130_assertion wasDerivedFrom befree-2016 NP736697.RAB2J9GI8KmRHaEGwiQT1Yq967QqHt35vwXLARoGZ5s6A130_provenance.
- NP736697.RAB2J9GI8KmRHaEGwiQT1Yq967QqHt35vwXLARoGZ5s6A130_assertion SIO_000772 19416273 NP736697.RAB2J9GI8KmRHaEGwiQT1Yq967QqHt35vwXLARoGZ5s6A130_provenance.
- NP736697.RAB2J9GI8KmRHaEGwiQT1Yq967QqHt35vwXLARoGZ5s6A130_assertion evidence source_evidence_literature NP736697.RAB2J9GI8KmRHaEGwiQT1Yq967QqHt35vwXLARoGZ5s6A130_provenance.
- NP736697.RAB2J9GI8KmRHaEGwiQT1Yq967QqHt35vwXLARoGZ5s6A130_assertion description "[Our results revealed that the A allele for SNP rs11104947 in the SCF gene and the T allele for SNP rs13866 in the SCGF gene were, respectively, associated with a 1.95- and a 2.14-fold risk of developing vitiligo vulgaris.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP736697.RAB2J9GI8KmRHaEGwiQT1Yq967QqHt35vwXLARoGZ5s6A130_provenance.