Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1400071.RAqVe8L3NBI5AGgaSAUuDa61uSSWC3f6fuTMGRC_vCwVw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1400071.RAqVe8L3NBI5AGgaSAUuDa61uSSWC3f6fuTMGRC_vCwVw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1400071.RAqVe8L3NBI5AGgaSAUuDa61uSSWC3f6fuTMGRC_vCwVw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1400071.RAqVe8L3NBI5AGgaSAUuDa61uSSWC3f6fuTMGRC_vCwVw130_provenance.
- NP1400071.RAqVe8L3NBI5AGgaSAUuDa61uSSWC3f6fuTMGRC_vCwVw130_assertion description "[We then compared colorectal cancers with 'mild' RER (n = 15), and those with 'severe' RER without (n = 11) or with (n = 22) detectable mutations in MSH2 or MLH1 to assess the involvement of mononucleotide repeats contained in the coding regions of MSH3, MSH6, BAX, and TGFbeta RII.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1400071.RAqVe8L3NBI5AGgaSAUuDa61uSSWC3f6fuTMGRC_vCwVw130_provenance.
- NP1400071.RAqVe8L3NBI5AGgaSAUuDa61uSSWC3f6fuTMGRC_vCwVw130_assertion evidence source_evidence_literature NP1400071.RAqVe8L3NBI5AGgaSAUuDa61uSSWC3f6fuTMGRC_vCwVw130_provenance.
- NP1400071.RAqVe8L3NBI5AGgaSAUuDa61uSSWC3f6fuTMGRC_vCwVw130_assertion SIO_000772 9674699 NP1400071.RAqVe8L3NBI5AGgaSAUuDa61uSSWC3f6fuTMGRC_vCwVw130_provenance.
- NP1400071.RAqVe8L3NBI5AGgaSAUuDa61uSSWC3f6fuTMGRC_vCwVw130_assertion wasDerivedFrom befree-2016 NP1400071.RAqVe8L3NBI5AGgaSAUuDa61uSSWC3f6fuTMGRC_vCwVw130_provenance.
- NP1400071.RAqVe8L3NBI5AGgaSAUuDa61uSSWC3f6fuTMGRC_vCwVw130_assertion wasGeneratedBy ECO_0000203 NP1400071.RAqVe8L3NBI5AGgaSAUuDa61uSSWC3f6fuTMGRC_vCwVw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1400071.RAqVe8L3NBI5AGgaSAUuDa61uSSWC3f6fuTMGRC_vCwVw130_provenance.