Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP692017.RA4fesVKiu4NH6GpOFjUgUlaGHqQRSh6gDz1dSZs9L0sg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP692017.RA4fesVKiu4NH6GpOFjUgUlaGHqQRSh6gDz1dSZs9L0sg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP692017.RA4fesVKiu4NH6GpOFjUgUlaGHqQRSh6gDz1dSZs9L0sg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP692017.RA4fesVKiu4NH6GpOFjUgUlaGHqQRSh6gDz1dSZs9L0sg130_provenance.
- NP692017.RA4fesVKiu4NH6GpOFjUgUlaGHqQRSh6gDz1dSZs9L0sg130_assertion description "[BRAF mutation and CIMP+ are therefore likely to be involved in an alternate, albeit rare, pathway to APC inactivation during the development of CRC in younger patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692017.RA4fesVKiu4NH6GpOFjUgUlaGHqQRSh6gDz1dSZs9L0sg130_provenance.
- NP692017.RA4fesVKiu4NH6GpOFjUgUlaGHqQRSh6gDz1dSZs9L0sg130_assertion evidence source_evidence_literature NP692017.RA4fesVKiu4NH6GpOFjUgUlaGHqQRSh6gDz1dSZs9L0sg130_provenance.
- NP692017.RA4fesVKiu4NH6GpOFjUgUlaGHqQRSh6gDz1dSZs9L0sg130_assertion SIO_000772 18778891 NP692017.RA4fesVKiu4NH6GpOFjUgUlaGHqQRSh6gDz1dSZs9L0sg130_provenance.
- NP692017.RA4fesVKiu4NH6GpOFjUgUlaGHqQRSh6gDz1dSZs9L0sg130_assertion wasDerivedFrom befree-2016 NP692017.RA4fesVKiu4NH6GpOFjUgUlaGHqQRSh6gDz1dSZs9L0sg130_provenance.
- NP692017.RA4fesVKiu4NH6GpOFjUgUlaGHqQRSh6gDz1dSZs9L0sg130_assertion wasGeneratedBy ECO_0000203 NP692017.RA4fesVKiu4NH6GpOFjUgUlaGHqQRSh6gDz1dSZs9L0sg130_provenance.
- befree-2016 importedOn "2016-02-19" NP692017.RA4fesVKiu4NH6GpOFjUgUlaGHqQRSh6gDz1dSZs9L0sg130_provenance.