Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP481645.RAYLlFzO3Pj5CKl02DKHJ1w7U8oyMqPe2uEGrZADIviNU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP481645.RAYLlFzO3Pj5CKl02DKHJ1w7U8oyMqPe2uEGrZADIviNU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP481645.RAYLlFzO3Pj5CKl02DKHJ1w7U8oyMqPe2uEGrZADIviNU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP481645.RAYLlFzO3Pj5CKl02DKHJ1w7U8oyMqPe2uEGrZADIviNU130_provenance.
- NP481645.RAYLlFzO3Pj5CKl02DKHJ1w7U8oyMqPe2uEGrZADIviNU130_assertion description "[We wished to determine genotype distributions for MTHFR 1298AC SNP in cases of MM and healthy controls and to examine whether there is any correlation between the methylation status of the CpG island of CDKN2A and Snk/Plk2 and MTHFR genotypes and with overall survival (OS) and other relevant clinical parameters.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP481645.RAYLlFzO3Pj5CKl02DKHJ1w7U8oyMqPe2uEGrZADIviNU130_provenance.
- NP481645.RAYLlFzO3Pj5CKl02DKHJ1w7U8oyMqPe2uEGrZADIviNU130_assertion evidence source_evidence_literature NP481645.RAYLlFzO3Pj5CKl02DKHJ1w7U8oyMqPe2uEGrZADIviNU130_provenance.
- NP481645.RAYLlFzO3Pj5CKl02DKHJ1w7U8oyMqPe2uEGrZADIviNU130_assertion SIO_000772 21067440 NP481645.RAYLlFzO3Pj5CKl02DKHJ1w7U8oyMqPe2uEGrZADIviNU130_provenance.
- NP481645.RAYLlFzO3Pj5CKl02DKHJ1w7U8oyMqPe2uEGrZADIviNU130_assertion wasDerivedFrom befree-20140225 NP481645.RAYLlFzO3Pj5CKl02DKHJ1w7U8oyMqPe2uEGrZADIviNU130_provenance.
- NP481645.RAYLlFzO3Pj5CKl02DKHJ1w7U8oyMqPe2uEGrZADIviNU130_assertion wasGeneratedBy ECO_0000203 NP481645.RAYLlFzO3Pj5CKl02DKHJ1w7U8oyMqPe2uEGrZADIviNU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP481645.RAYLlFzO3Pj5CKl02DKHJ1w7U8oyMqPe2uEGrZADIviNU130_provenance.