Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1240484.RAY5dfvwFV8-8cCEH1LEpTxTdYiN4GMujf17uc4pGoAeA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1240484.RAY5dfvwFV8-8cCEH1LEpTxTdYiN4GMujf17uc4pGoAeA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1240484.RAY5dfvwFV8-8cCEH1LEpTxTdYiN4GMujf17uc4pGoAeA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1240484.RAY5dfvwFV8-8cCEH1LEpTxTdYiN4GMujf17uc4pGoAeA130_provenance.
- NP1240484.RAY5dfvwFV8-8cCEH1LEpTxTdYiN4GMujf17uc4pGoAeA130_assertion description "[Compound heterozygosity for a frame shift mutation and a likely pathogenic sequence variant in the planar cell polarity?ciliogenesis gene WDPCP in a girl with polysyndactyly, coarctation of the aorta, and tongue hamartomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1240484.RAY5dfvwFV8-8cCEH1LEpTxTdYiN4GMujf17uc4pGoAeA130_provenance.
- NP1240484.RAY5dfvwFV8-8cCEH1LEpTxTdYiN4GMujf17uc4pGoAeA130_assertion evidence source_evidence_literature NP1240484.RAY5dfvwFV8-8cCEH1LEpTxTdYiN4GMujf17uc4pGoAeA130_provenance.
- NP1240484.RAY5dfvwFV8-8cCEH1LEpTxTdYiN4GMujf17uc4pGoAeA130_assertion SIO_000772 25427950 NP1240484.RAY5dfvwFV8-8cCEH1LEpTxTdYiN4GMujf17uc4pGoAeA130_provenance.
- NP1240484.RAY5dfvwFV8-8cCEH1LEpTxTdYiN4GMujf17uc4pGoAeA130_assertion wasDerivedFrom befree-2016 NP1240484.RAY5dfvwFV8-8cCEH1LEpTxTdYiN4GMujf17uc4pGoAeA130_provenance.
- NP1240484.RAY5dfvwFV8-8cCEH1LEpTxTdYiN4GMujf17uc4pGoAeA130_assertion wasGeneratedBy ECO_0000203 NP1240484.RAY5dfvwFV8-8cCEH1LEpTxTdYiN4GMujf17uc4pGoAeA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1240484.RAY5dfvwFV8-8cCEH1LEpTxTdYiN4GMujf17uc4pGoAeA130_provenance.