Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP119956.RAWf1aX2PXJnJLJGscmobQBF1I-vyeUML7Rz58qaK1SLw130_assertion> ?p ?o ?g. }
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- NP119956.RAWf1aX2PXJnJLJGscmobQBF1I-vyeUML7Rz58qaK1SLw130_assertion type Assertion NP119956.RAWf1aX2PXJnJLJGscmobQBF1I-vyeUML7Rz58qaK1SLw130_head.
- NP119956.RAWf1aX2PXJnJLJGscmobQBF1I-vyeUML7Rz58qaK1SLw130_assertion description "[Neither the VDR C352T nor the MPO G463A genotype had manifested association with the dysplasia and carcinoma of the disease, whereas the MTHFR 677TT genotype may be a genetic risk factor for esophageal dysplasia and carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP119956.RAWf1aX2PXJnJLJGscmobQBF1I-vyeUML7Rz58qaK1SLw130_provenance.
- NP119956.RAWf1aX2PXJnJLJGscmobQBF1I-vyeUML7Rz58qaK1SLw130_assertion evidence source_evidence_literature NP119956.RAWf1aX2PXJnJLJGscmobQBF1I-vyeUML7Rz58qaK1SLw130_provenance.
- NP119956.RAWf1aX2PXJnJLJGscmobQBF1I-vyeUML7Rz58qaK1SLw130_assertion SIO_000772 18662591 NP119956.RAWf1aX2PXJnJLJGscmobQBF1I-vyeUML7Rz58qaK1SLw130_provenance.
- NP119956.RAWf1aX2PXJnJLJGscmobQBF1I-vyeUML7Rz58qaK1SLw130_assertion wasDerivedFrom gad-20150221 NP119956.RAWf1aX2PXJnJLJGscmobQBF1I-vyeUML7Rz58qaK1SLw130_provenance.
- NP119956.RAWf1aX2PXJnJLJGscmobQBF1I-vyeUML7Rz58qaK1SLw130_assertion wasGeneratedBy ECO_0000203 NP119956.RAWf1aX2PXJnJLJGscmobQBF1I-vyeUML7Rz58qaK1SLw130_provenance.