Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP953815.RAFtwVvhah_so3X78ktbxQWfpSSDQ8FPpXRGqUjzKZ0z8130_assertion> ?p ?o ?g. }
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- NP953815.RAFtwVvhah_so3X78ktbxQWfpSSDQ8FPpXRGqUjzKZ0z8130_assertion type Assertion NP953815.RAFtwVvhah_so3X78ktbxQWfpSSDQ8FPpXRGqUjzKZ0z8130_head.
- 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.