Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP501632.RAbjwyCNqlqNRoQHVCYCdtNMS6gFzQrBIiVYhNddZJkJE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP501632.RAbjwyCNqlqNRoQHVCYCdtNMS6gFzQrBIiVYhNddZJkJE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP501632.RAbjwyCNqlqNRoQHVCYCdtNMS6gFzQrBIiVYhNddZJkJE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP501632.RAbjwyCNqlqNRoQHVCYCdtNMS6gFzQrBIiVYhNddZJkJE130_provenance.
- NP501632.RAbjwyCNqlqNRoQHVCYCdtNMS6gFzQrBIiVYhNddZJkJE130_assertion description "[The Y165C and 1103delC mutations significantly reduce MUTYH protein stability and thus repair activity, whereas the G382D mutation produces dysfunctional protein only suggesting different functional molecular mechanisms by which the MAP phenotype may contribute to the development of CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP501632.RAbjwyCNqlqNRoQHVCYCdtNMS6gFzQrBIiVYhNddZJkJE130_provenance.
- NP501632.RAbjwyCNqlqNRoQHVCYCdtNMS6gFzQrBIiVYhNddZJkJE130_assertion evidence source_evidence_literature NP501632.RAbjwyCNqlqNRoQHVCYCdtNMS6gFzQrBIiVYhNddZJkJE130_provenance.
- NP501632.RAbjwyCNqlqNRoQHVCYCdtNMS6gFzQrBIiVYhNddZJkJE130_assertion SIO_000772 15987719 NP501632.RAbjwyCNqlqNRoQHVCYCdtNMS6gFzQrBIiVYhNddZJkJE130_provenance.
- NP501632.RAbjwyCNqlqNRoQHVCYCdtNMS6gFzQrBIiVYhNddZJkJE130_assertion wasDerivedFrom befree-2016 NP501632.RAbjwyCNqlqNRoQHVCYCdtNMS6gFzQrBIiVYhNddZJkJE130_provenance.
- NP501632.RAbjwyCNqlqNRoQHVCYCdtNMS6gFzQrBIiVYhNddZJkJE130_assertion wasGeneratedBy ECO_0000203 NP501632.RAbjwyCNqlqNRoQHVCYCdtNMS6gFzQrBIiVYhNddZJkJE130_provenance.
- befree-2016 importedOn "2016-02-19" NP501632.RAbjwyCNqlqNRoQHVCYCdtNMS6gFzQrBIiVYhNddZJkJE130_provenance.