Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP629368.RA8-2UrKVHM-EPGCQNJ3DuwQ9lSNUFz1Hw7-nJMDiv4dQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP629368.RA8-2UrKVHM-EPGCQNJ3DuwQ9lSNUFz1Hw7-nJMDiv4dQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP629368.RA8-2UrKVHM-EPGCQNJ3DuwQ9lSNUFz1Hw7-nJMDiv4dQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP629368.RA8-2UrKVHM-EPGCQNJ3DuwQ9lSNUFz1Hw7-nJMDiv4dQ130_provenance.
- NP629368.RA8-2UrKVHM-EPGCQNJ3DuwQ9lSNUFz1Hw7-nJMDiv4dQ130_assertion description "[Involvement of the genes on 5q (FAP) and 18q (Lynch syndrome II) in hereditary colon cancer syndromes is supported by linkage studies, but their respective roles (as well as that of the gene on 17p) in familial and sporadic colorectal cancer remain to be precisely defined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP629368.RA8-2UrKVHM-EPGCQNJ3DuwQ9lSNUFz1Hw7-nJMDiv4dQ130_provenance.
- NP629368.RA8-2UrKVHM-EPGCQNJ3DuwQ9lSNUFz1Hw7-nJMDiv4dQ130_assertion evidence source_evidence_literature NP629368.RA8-2UrKVHM-EPGCQNJ3DuwQ9lSNUFz1Hw7-nJMDiv4dQ130_provenance.
- NP629368.RA8-2UrKVHM-EPGCQNJ3DuwQ9lSNUFz1Hw7-nJMDiv4dQ130_assertion SIO_000772 2645266 NP629368.RA8-2UrKVHM-EPGCQNJ3DuwQ9lSNUFz1Hw7-nJMDiv4dQ130_provenance.
- NP629368.RA8-2UrKVHM-EPGCQNJ3DuwQ9lSNUFz1Hw7-nJMDiv4dQ130_assertion wasDerivedFrom befree-20140225 NP629368.RA8-2UrKVHM-EPGCQNJ3DuwQ9lSNUFz1Hw7-nJMDiv4dQ130_provenance.
- NP629368.RA8-2UrKVHM-EPGCQNJ3DuwQ9lSNUFz1Hw7-nJMDiv4dQ130_assertion wasGeneratedBy ECO_0000203 NP629368.RA8-2UrKVHM-EPGCQNJ3DuwQ9lSNUFz1Hw7-nJMDiv4dQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP629368.RA8-2UrKVHM-EPGCQNJ3DuwQ9lSNUFz1Hw7-nJMDiv4dQ130_provenance.