Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP690770.RA2L-rFj8vUVWiFaLeTSaTkoYpGmkdVn850y6eJj7nj-Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP690770.RA2L-rFj8vUVWiFaLeTSaTkoYpGmkdVn850y6eJj7nj-Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690770.RA2L-rFj8vUVWiFaLeTSaTkoYpGmkdVn850y6eJj7nj-Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690770.RA2L-rFj8vUVWiFaLeTSaTkoYpGmkdVn850y6eJj7nj-Q130_provenance.
- NP690770.RA2L-rFj8vUVWiFaLeTSaTkoYpGmkdVn850y6eJj7nj-Q130_assertion description "[The 10p15.3-p15.1 has not been reported to be linked to hereditary CRC in previous linkage studies, but this region does harbour the Kruppel-like factor 6 (KLF6) gene that is known to be altered in common CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690770.RA2L-rFj8vUVWiFaLeTSaTkoYpGmkdVn850y6eJj7nj-Q130_provenance.
- NP690770.RA2L-rFj8vUVWiFaLeTSaTkoYpGmkdVn850y6eJj7nj-Q130_assertion evidence source_evidence_literature NP690770.RA2L-rFj8vUVWiFaLeTSaTkoYpGmkdVn850y6eJj7nj-Q130_provenance.
- NP690770.RA2L-rFj8vUVWiFaLeTSaTkoYpGmkdVn850y6eJj7nj-Q130_assertion SIO_000772 21829229 NP690770.RA2L-rFj8vUVWiFaLeTSaTkoYpGmkdVn850y6eJj7nj-Q130_provenance.
- NP690770.RA2L-rFj8vUVWiFaLeTSaTkoYpGmkdVn850y6eJj7nj-Q130_assertion wasDerivedFrom befree-20140225 NP690770.RA2L-rFj8vUVWiFaLeTSaTkoYpGmkdVn850y6eJj7nj-Q130_provenance.
- NP690770.RA2L-rFj8vUVWiFaLeTSaTkoYpGmkdVn850y6eJj7nj-Q130_assertion wasGeneratedBy ECO_0000203 NP690770.RA2L-rFj8vUVWiFaLeTSaTkoYpGmkdVn850y6eJj7nj-Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP690770.RA2L-rFj8vUVWiFaLeTSaTkoYpGmkdVn850y6eJj7nj-Q130_provenance.