Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP48560.RAnV7Kt9-uhyly_QHPhKBArXlQ8RXBHUes2fBhw-aTuCA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP48560.RAnV7Kt9-uhyly_QHPhKBArXlQ8RXBHUes2fBhw-aTuCA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP48560.RAnV7Kt9-uhyly_QHPhKBArXlQ8RXBHUes2fBhw-aTuCA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP48560.RAnV7Kt9-uhyly_QHPhKBArXlQ8RXBHUes2fBhw-aTuCA130_provenance.
- NP48560.RAnV7Kt9-uhyly_QHPhKBArXlQ8RXBHUes2fBhw-aTuCA130_assertion wasGeneratedBy ECO_0000203 NP48560.RAnV7Kt9-uhyly_QHPhKBArXlQ8RXBHUes2fBhw-aTuCA130_provenance.
- NP48560.RAnV7Kt9-uhyly_QHPhKBArXlQ8RXBHUes2fBhw-aTuCA130_assertion wasDerivedFrom gad-20130706 NP48560.RAnV7Kt9-uhyly_QHPhKBArXlQ8RXBHUes2fBhw-aTuCA130_provenance.
- NP48560.RAnV7Kt9-uhyly_QHPhKBArXlQ8RXBHUes2fBhw-aTuCA130_assertion SIO_000772 14724162 NP48560.RAnV7Kt9-uhyly_QHPhKBArXlQ8RXBHUes2fBhw-aTuCA130_provenance.
- NP48560.RAnV7Kt9-uhyly_QHPhKBArXlQ8RXBHUes2fBhw-aTuCA130_assertion evidence source_evidence_literature NP48560.RAnV7Kt9-uhyly_QHPhKBArXlQ8RXBHUes2fBhw-aTuCA130_provenance.
- NP48560.RAnV7Kt9-uhyly_QHPhKBArXlQ8RXBHUes2fBhw-aTuCA130_assertion description "[The severe phenotype should be considered when counselling FAP families in which attenuated FAP is excluded and in which a causative APC mutation has not been identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48560.RAnV7Kt9-uhyly_QHPhKBArXlQ8RXBHUes2fBhw-aTuCA130_provenance.
- gad-20130706 importedOn "2013-07-06" NP48560.RAnV7Kt9-uhyly_QHPhKBArXlQ8RXBHUes2fBhw-aTuCA130_provenance.