Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1404171.RA8qN5gED96nSWm4_PI5TeL7-kyUenJ9gsvUrW2tsaX5s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1404171.RA8qN5gED96nSWm4_PI5TeL7-kyUenJ9gsvUrW2tsaX5s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1404171.RA8qN5gED96nSWm4_PI5TeL7-kyUenJ9gsvUrW2tsaX5s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1404171.RA8qN5gED96nSWm4_PI5TeL7-kyUenJ9gsvUrW2tsaX5s130_provenance.
- NP1404171.RA8qN5gED96nSWm4_PI5TeL7-kyUenJ9gsvUrW2tsaX5s130_assertion description "[The detection rate was 10/48 (20.8 per cent) in the presence of VSD, ASD2 or combined ASD2 + VSD, the detection rate was 29/39 (74.3 per cent) in the presence of other forms of congenital heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1404171.RA8qN5gED96nSWm4_PI5TeL7-kyUenJ9gsvUrW2tsaX5s130_provenance.
- NP1404171.RA8qN5gED96nSWm4_PI5TeL7-kyUenJ9gsvUrW2tsaX5s130_assertion evidence source_evidence_literature NP1404171.RA8qN5gED96nSWm4_PI5TeL7-kyUenJ9gsvUrW2tsaX5s130_provenance.
- NP1404171.RA8qN5gED96nSWm4_PI5TeL7-kyUenJ9gsvUrW2tsaX5s130_assertion SIO_000772 9742568 NP1404171.RA8qN5gED96nSWm4_PI5TeL7-kyUenJ9gsvUrW2tsaX5s130_provenance.
- NP1404171.RA8qN5gED96nSWm4_PI5TeL7-kyUenJ9gsvUrW2tsaX5s130_assertion wasDerivedFrom befree-2016 NP1404171.RA8qN5gED96nSWm4_PI5TeL7-kyUenJ9gsvUrW2tsaX5s130_provenance.
- NP1404171.RA8qN5gED96nSWm4_PI5TeL7-kyUenJ9gsvUrW2tsaX5s130_assertion wasGeneratedBy ECO_0000203 NP1404171.RA8qN5gED96nSWm4_PI5TeL7-kyUenJ9gsvUrW2tsaX5s130_provenance.
- befree-2016 importedOn "2016-02-19" NP1404171.RA8qN5gED96nSWm4_PI5TeL7-kyUenJ9gsvUrW2tsaX5s130_provenance.