Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP953815.RAFtwVvhah_so3X78ktbxQWfpSSDQ8FPpXRGqUjzKZ0z8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP953815.RAFtwVvhah_so3X78ktbxQWfpSSDQ8FPpXRGqUjzKZ0z8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP953815.RAFtwVvhah_so3X78ktbxQWfpSSDQ8FPpXRGqUjzKZ0z8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP953815.RAFtwVvhah_so3X78ktbxQWfpSSDQ8FPpXRGqUjzKZ0z8130_provenance.
- NP953815.RAFtwVvhah_so3X78ktbxQWfpSSDQ8FPpXRGqUjzKZ0z8130_assertion description "[Furthermore, individuals carrying one or two MC1R nonsynonymous changes and GSTP1 rs1695 rare allele had an increased risk of developing MM (OR: 3�34, 95% CI: 1�42-8�09 and OR: 20�42, 95% CI: 2�80-417�42, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP953815.RAFtwVvhah_so3X78ktbxQWfpSSDQ8FPpXRGqUjzKZ0z8130_provenance.
- NP953815.RAFtwVvhah_so3X78ktbxQWfpSSDQ8FPpXRGqUjzKZ0z8130_assertion evidence source_evidence_literature NP953815.RAFtwVvhah_so3X78ktbxQWfpSSDQ8FPpXRGqUjzKZ0z8130_provenance.
- NP953815.RAFtwVvhah_so3X78ktbxQWfpSSDQ8FPpXRGqUjzKZ0z8130_assertion SIO_000772 22251241 NP953815.RAFtwVvhah_so3X78ktbxQWfpSSDQ8FPpXRGqUjzKZ0z8130_provenance.
- NP953815.RAFtwVvhah_so3X78ktbxQWfpSSDQ8FPpXRGqUjzKZ0z8130_assertion wasDerivedFrom befree-2016 NP953815.RAFtwVvhah_so3X78ktbxQWfpSSDQ8FPpXRGqUjzKZ0z8130_provenance.
- NP953815.RAFtwVvhah_so3X78ktbxQWfpSSDQ8FPpXRGqUjzKZ0z8130_assertion wasGeneratedBy ECO_0000203 NP953815.RAFtwVvhah_so3X78ktbxQWfpSSDQ8FPpXRGqUjzKZ0z8130_provenance.
- befree-2016 importedOn "2016-02-19" NP953815.RAFtwVvhah_so3X78ktbxQWfpSSDQ8FPpXRGqUjzKZ0z8130_provenance.