Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP870778.RANUdlZpsV45W3mYrpcF3BAWaKm1NT9UjH3YgoQSwSs_E130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP870778.RANUdlZpsV45W3mYrpcF3BAWaKm1NT9UjH3YgoQSwSs_E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP870778.RANUdlZpsV45W3mYrpcF3BAWaKm1NT9UjH3YgoQSwSs_E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP870778.RANUdlZpsV45W3mYrpcF3BAWaKm1NT9UjH3YgoQSwSs_E130_provenance.
- NP870778.RANUdlZpsV45W3mYrpcF3BAWaKm1NT9UjH3YgoQSwSs_E130_assertion description "[A variant in the carboxyl-terminus of connexin 40 alters GAP junctions and increases risk for tetralogy of Fallot.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870778.RANUdlZpsV45W3mYrpcF3BAWaKm1NT9UjH3YgoQSwSs_E130_provenance.
- NP870778.RANUdlZpsV45W3mYrpcF3BAWaKm1NT9UjH3YgoQSwSs_E130_assertion evidence source_evidence_literature NP870778.RANUdlZpsV45W3mYrpcF3BAWaKm1NT9UjH3YgoQSwSs_E130_provenance.
- NP870778.RANUdlZpsV45W3mYrpcF3BAWaKm1NT9UjH3YgoQSwSs_E130_assertion SIO_000772 22713807 NP870778.RANUdlZpsV45W3mYrpcF3BAWaKm1NT9UjH3YgoQSwSs_E130_provenance.
- NP870778.RANUdlZpsV45W3mYrpcF3BAWaKm1NT9UjH3YgoQSwSs_E130_assertion wasDerivedFrom befree-20140225 NP870778.RANUdlZpsV45W3mYrpcF3BAWaKm1NT9UjH3YgoQSwSs_E130_provenance.
- NP870778.RANUdlZpsV45W3mYrpcF3BAWaKm1NT9UjH3YgoQSwSs_E130_assertion wasGeneratedBy ECO_0000203 NP870778.RANUdlZpsV45W3mYrpcF3BAWaKm1NT9UjH3YgoQSwSs_E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP870778.RANUdlZpsV45W3mYrpcF3BAWaKm1NT9UjH3YgoQSwSs_E130_provenance.