Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP782392.RAiaFZQHhAQ3a5Oj3r8Dp4xRNRpAzzdnlWGBljQ7uz4ho130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP782392.RAiaFZQHhAQ3a5Oj3r8Dp4xRNRpAzzdnlWGBljQ7uz4ho130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP782392.RAiaFZQHhAQ3a5Oj3r8Dp4xRNRpAzzdnlWGBljQ7uz4ho130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP782392.RAiaFZQHhAQ3a5Oj3r8Dp4xRNRpAzzdnlWGBljQ7uz4ho130_provenance.
- NP782392.RAiaFZQHhAQ3a5Oj3r8Dp4xRNRpAzzdnlWGBljQ7uz4ho130_assertion description "[The hereditary colon and endometrium cancer predisposition Lynch Syndrome (also called HNPCC) is caused by a germ-line mutation in one of the DNA mismatch repair (MMR) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782392.RAiaFZQHhAQ3a5Oj3r8Dp4xRNRpAzzdnlWGBljQ7uz4ho130_provenance.
- NP782392.RAiaFZQHhAQ3a5Oj3r8Dp4xRNRpAzzdnlWGBljQ7uz4ho130_assertion evidence source_evidence_literature NP782392.RAiaFZQHhAQ3a5Oj3r8Dp4xRNRpAzzdnlWGBljQ7uz4ho130_provenance.
- NP782392.RAiaFZQHhAQ3a5Oj3r8Dp4xRNRpAzzdnlWGBljQ7uz4ho130_assertion SIO_000772 20020535 NP782392.RAiaFZQHhAQ3a5Oj3r8Dp4xRNRpAzzdnlWGBljQ7uz4ho130_provenance.
- NP782392.RAiaFZQHhAQ3a5Oj3r8Dp4xRNRpAzzdnlWGBljQ7uz4ho130_assertion wasDerivedFrom befree-2016 NP782392.RAiaFZQHhAQ3a5Oj3r8Dp4xRNRpAzzdnlWGBljQ7uz4ho130_provenance.
- NP782392.RAiaFZQHhAQ3a5Oj3r8Dp4xRNRpAzzdnlWGBljQ7uz4ho130_assertion wasGeneratedBy ECO_0000203 NP782392.RAiaFZQHhAQ3a5Oj3r8Dp4xRNRpAzzdnlWGBljQ7uz4ho130_provenance.
- befree-2016 importedOn "2016-02-19" NP782392.RAiaFZQHhAQ3a5Oj3r8Dp4xRNRpAzzdnlWGBljQ7uz4ho130_provenance.