Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP811113.RA31p9Jw5VHQ9bty_Lk3Zan_6bHOKXGv2k7RHefnbtnk8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP811113.RA31p9Jw5VHQ9bty_Lk3Zan_6bHOKXGv2k7RHefnbtnk8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP811113.RA31p9Jw5VHQ9bty_Lk3Zan_6bHOKXGv2k7RHefnbtnk8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP811113.RA31p9Jw5VHQ9bty_Lk3Zan_6bHOKXGv2k7RHefnbtnk8130_provenance.
- NP811113.RA31p9Jw5VHQ9bty_Lk3Zan_6bHOKXGv2k7RHefnbtnk8130_assertion description "[We report here a novel mechanism that a mutation in the MLH1 3'-untranslated region (3'-UTR) leads to MMR deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP811113.RA31p9Jw5VHQ9bty_Lk3Zan_6bHOKXGv2k7RHefnbtnk8130_provenance.
- NP811113.RA31p9Jw5VHQ9bty_Lk3Zan_6bHOKXGv2k7RHefnbtnk8130_assertion evidence source_evidence_literature NP811113.RA31p9Jw5VHQ9bty_Lk3Zan_6bHOKXGv2k7RHefnbtnk8130_provenance.
- NP811113.RA31p9Jw5VHQ9bty_Lk3Zan_6bHOKXGv2k7RHefnbtnk8130_assertion SIO_000772 18056700 NP811113.RA31p9Jw5VHQ9bty_Lk3Zan_6bHOKXGv2k7RHefnbtnk8130_provenance.
- NP811113.RA31p9Jw5VHQ9bty_Lk3Zan_6bHOKXGv2k7RHefnbtnk8130_assertion wasDerivedFrom befree-20140225 NP811113.RA31p9Jw5VHQ9bty_Lk3Zan_6bHOKXGv2k7RHefnbtnk8130_provenance.
- NP811113.RA31p9Jw5VHQ9bty_Lk3Zan_6bHOKXGv2k7RHefnbtnk8130_assertion wasGeneratedBy ECO_0000203 NP811113.RA31p9Jw5VHQ9bty_Lk3Zan_6bHOKXGv2k7RHefnbtnk8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP811113.RA31p9Jw5VHQ9bty_Lk3Zan_6bHOKXGv2k7RHefnbtnk8130_provenance.