Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP782272.RAVcxF5OMFYAIZLT3NZL7v9UEjby31PuO56if7KU4fE5Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP782272.RAVcxF5OMFYAIZLT3NZL7v9UEjby31PuO56if7KU4fE5Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP782272.RAVcxF5OMFYAIZLT3NZL7v9UEjby31PuO56if7KU4fE5Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP782272.RAVcxF5OMFYAIZLT3NZL7v9UEjby31PuO56if7KU4fE5Q130_provenance.
- NP782272.RAVcxF5OMFYAIZLT3NZL7v9UEjby31PuO56if7KU4fE5Q130_assertion description "[Some evidence exists for the effects of X-ray cross complementation group 1 (XRCC1) codon 280 and (in smokers) Xeroderma pigmentosum group D (XPD) codon 23 polymorphisms on baseline CAs, for XRCC1 codon 399 polymorphism on SCEs in smokers, and for methylene tetrahydrofolate reductase (MTHFR) codon 677 and methionine synthase reductase (MTRR) polymorphisms on spontaneous MN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782272.RAVcxF5OMFYAIZLT3NZL7v9UEjby31PuO56if7KU4fE5Q130_provenance.
- NP782272.RAVcxF5OMFYAIZLT3NZL7v9UEjby31PuO56if7KU4fE5Q130_assertion evidence source_evidence_literature NP782272.RAVcxF5OMFYAIZLT3NZL7v9UEjby31PuO56if7KU4fE5Q130_provenance.
- NP782272.RAVcxF5OMFYAIZLT3NZL7v9UEjby31PuO56if7KU4fE5Q130_assertion SIO_000772 15093278 NP782272.RAVcxF5OMFYAIZLT3NZL7v9UEjby31PuO56if7KU4fE5Q130_provenance.
- NP782272.RAVcxF5OMFYAIZLT3NZL7v9UEjby31PuO56if7KU4fE5Q130_assertion wasDerivedFrom befree-20140225 NP782272.RAVcxF5OMFYAIZLT3NZL7v9UEjby31PuO56if7KU4fE5Q130_provenance.
- NP782272.RAVcxF5OMFYAIZLT3NZL7v9UEjby31PuO56if7KU4fE5Q130_assertion wasGeneratedBy ECO_0000203 NP782272.RAVcxF5OMFYAIZLT3NZL7v9UEjby31PuO56if7KU4fE5Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP782272.RAVcxF5OMFYAIZLT3NZL7v9UEjby31PuO56if7KU4fE5Q130_provenance.