Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_provenance.
- NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_assertion description "[The CHEK2 1100delC was not significantly increased in Swedish colorectal cancer patients, however, in order to determine the role of the variant in colorectal cancer families with the history of breast cancer a larger sample size is needed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_provenance.
- NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_assertion evidence source_evidence_literature NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_provenance.
- NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_assertion SIO_000772 17214356 NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_provenance.
- NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_assertion wasDerivedFrom gad-20130706 NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_provenance.
- NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_assertion wasGeneratedBy ECO_0000203 NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_provenance.
- gad-20130706 importedOn "2013-07-06" NP46806.RA80c4fFXhaiG-OL7lnfKNhwR1U8ETADYcessVnHWCR3k130_provenance.