Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP715610.RAWSPwKNuKYlJKUm4sQZ93ApWT1zIzqC5NkXKCcfAMhGI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP715610.RAWSPwKNuKYlJKUm4sQZ93ApWT1zIzqC5NkXKCcfAMhGI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP715610.RAWSPwKNuKYlJKUm4sQZ93ApWT1zIzqC5NkXKCcfAMhGI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP715610.RAWSPwKNuKYlJKUm4sQZ93ApWT1zIzqC5NkXKCcfAMhGI130_provenance.
- NP715610.RAWSPwKNuKYlJKUm4sQZ93ApWT1zIzqC5NkXKCcfAMhGI130_assertion description "[Two common single nucleotide polymorphisms (SNPs) located within the MTHFR gene, 677 C>T and 1298 A>C, that alter the function of the encoded protein have been the focus of many studies on CRC risk outside the context of an inherited predisposition to disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715610.RAWSPwKNuKYlJKUm4sQZ93ApWT1zIzqC5NkXKCcfAMhGI130_provenance.
- NP715610.RAWSPwKNuKYlJKUm4sQZ93ApWT1zIzqC5NkXKCcfAMhGI130_assertion evidence source_evidence_literature NP715610.RAWSPwKNuKYlJKUm4sQZ93ApWT1zIzqC5NkXKCcfAMhGI130_provenance.
- NP715610.RAWSPwKNuKYlJKUm4sQZ93ApWT1zIzqC5NkXKCcfAMhGI130_assertion SIO_000772 19156174 NP715610.RAWSPwKNuKYlJKUm4sQZ93ApWT1zIzqC5NkXKCcfAMhGI130_provenance.
- NP715610.RAWSPwKNuKYlJKUm4sQZ93ApWT1zIzqC5NkXKCcfAMhGI130_assertion wasDerivedFrom befree-2016 NP715610.RAWSPwKNuKYlJKUm4sQZ93ApWT1zIzqC5NkXKCcfAMhGI130_provenance.
- NP715610.RAWSPwKNuKYlJKUm4sQZ93ApWT1zIzqC5NkXKCcfAMhGI130_assertion wasGeneratedBy ECO_0000203 NP715610.RAWSPwKNuKYlJKUm4sQZ93ApWT1zIzqC5NkXKCcfAMhGI130_provenance.
- befree-2016 importedOn "2016-02-19" NP715610.RAWSPwKNuKYlJKUm4sQZ93ApWT1zIzqC5NkXKCcfAMhGI130_provenance.