Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP523016.RA5b86w-hT1KNUEgAGYP4TWfaZcDHTt8nT5mzLfve06lg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP523016.RA5b86w-hT1KNUEgAGYP4TWfaZcDHTt8nT5mzLfve06lg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP523016.RA5b86w-hT1KNUEgAGYP4TWfaZcDHTt8nT5mzLfve06lg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP523016.RA5b86w-hT1KNUEgAGYP4TWfaZcDHTt8nT5mzLfve06lg130_provenance.
- befree-2016 importedOn "2016-02-19" NP523016.RA5b86w-hT1KNUEgAGYP4TWfaZcDHTt8nT5mzLfve06lg130_provenance.
- NP523016.RA5b86w-hT1KNUEgAGYP4TWfaZcDHTt8nT5mzLfve06lg130_assertion wasGeneratedBy ECO_0000203 NP523016.RA5b86w-hT1KNUEgAGYP4TWfaZcDHTt8nT5mzLfve06lg130_provenance.
- NP523016.RA5b86w-hT1KNUEgAGYP4TWfaZcDHTt8nT5mzLfve06lg130_assertion wasDerivedFrom befree-2016 NP523016.RA5b86w-hT1KNUEgAGYP4TWfaZcDHTt8nT5mzLfve06lg130_provenance.
- NP523016.RA5b86w-hT1KNUEgAGYP4TWfaZcDHTt8nT5mzLfve06lg130_assertion SIO_000772 16292097 NP523016.RA5b86w-hT1KNUEgAGYP4TWfaZcDHTt8nT5mzLfve06lg130_provenance.
- NP523016.RA5b86w-hT1KNUEgAGYP4TWfaZcDHTt8nT5mzLfve06lg130_assertion evidence source_evidence_literature NP523016.RA5b86w-hT1KNUEgAGYP4TWfaZcDHTt8nT5mzLfve06lg130_provenance.
- NP523016.RA5b86w-hT1KNUEgAGYP4TWfaZcDHTt8nT5mzLfve06lg130_assertion description "[We identified a mutation in the APC gene that results in a truncated protein (Y935X) in the FAP proband, and subsequently in 12 FAP-affected members.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523016.RA5b86w-hT1KNUEgAGYP4TWfaZcDHTt8nT5mzLfve06lg130_provenance.