Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP189932.RAzjrH7IDyE3fBPKNjjcCU0MyzuwHX_Q4uJ7RdXMkrVTc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP189932.RAzjrH7IDyE3fBPKNjjcCU0MyzuwHX_Q4uJ7RdXMkrVTc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP189932.RAzjrH7IDyE3fBPKNjjcCU0MyzuwHX_Q4uJ7RdXMkrVTc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP189932.RAzjrH7IDyE3fBPKNjjcCU0MyzuwHX_Q4uJ7RdXMkrVTc130_provenance.
- NP189932.RAzjrH7IDyE3fBPKNjjcCU0MyzuwHX_Q4uJ7RdXMkrVTc130_assertion description "[This study implicates nine different loci involved in genetic susceptibility to Dupuytrens disease. The fact that six of these nine loci harbor genes encoding proteins in the Wnt-signaling pathway suggests that aberrations in this pathway are key to the p]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP189932.RAzjrH7IDyE3fBPKNjjcCU0MyzuwHX_Q4uJ7RdXMkrVTc130_provenance.
- NP189932.RAzjrH7IDyE3fBPKNjjcCU0MyzuwHX_Q4uJ7RdXMkrVTc130_assertion evidence source_evidence_literature NP189932.RAzjrH7IDyE3fBPKNjjcCU0MyzuwHX_Q4uJ7RdXMkrVTc130_provenance.
- NP189932.RAzjrH7IDyE3fBPKNjjcCU0MyzuwHX_Q4uJ7RdXMkrVTc130_assertion SIO_000772 21732829 NP189932.RAzjrH7IDyE3fBPKNjjcCU0MyzuwHX_Q4uJ7RdXMkrVTc130_provenance.
- NP189932.RAzjrH7IDyE3fBPKNjjcCU0MyzuwHX_Q4uJ7RdXMkrVTc130_assertion wasDerivedFrom gad-20150221 NP189932.RAzjrH7IDyE3fBPKNjjcCU0MyzuwHX_Q4uJ7RdXMkrVTc130_provenance.
- NP189932.RAzjrH7IDyE3fBPKNjjcCU0MyzuwHX_Q4uJ7RdXMkrVTc130_assertion wasGeneratedBy ECO_0000203 NP189932.RAzjrH7IDyE3fBPKNjjcCU0MyzuwHX_Q4uJ7RdXMkrVTc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP189932.RAzjrH7IDyE3fBPKNjjcCU0MyzuwHX_Q4uJ7RdXMkrVTc130_provenance.