Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP224329.RAWsckq267gTDqbtHyNpQhg426g6h2GCsNig3Ml0zZ_nQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP224329.RAWsckq267gTDqbtHyNpQhg426g6h2GCsNig3Ml0zZ_nQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP224329.RAWsckq267gTDqbtHyNpQhg426g6h2GCsNig3Ml0zZ_nQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP224329.RAWsckq267gTDqbtHyNpQhg426g6h2GCsNig3Ml0zZ_nQ130_provenance.
- NP224329.RAWsckq267gTDqbtHyNpQhg426g6h2GCsNig3Ml0zZ_nQ130_assertion description "[Together with our previous results, we found 27 germline mutations of SDH genes in 95 cases (28%) of sporadic head and neck paraganglioma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP224329.RAWsckq267gTDqbtHyNpQhg426g6h2GCsNig3Ml0zZ_nQ130_provenance.
- NP224329.RAWsckq267gTDqbtHyNpQhg426g6h2GCsNig3Ml0zZ_nQ130_assertion evidence source_evidence_literature NP224329.RAWsckq267gTDqbtHyNpQhg426g6h2GCsNig3Ml0zZ_nQ130_provenance.
- NP224329.RAWsckq267gTDqbtHyNpQhg426g6h2GCsNig3Ml0zZ_nQ130_assertion SIO_000772 16405730 NP224329.RAWsckq267gTDqbtHyNpQhg426g6h2GCsNig3Ml0zZ_nQ130_provenance.
- NP224329.RAWsckq267gTDqbtHyNpQhg426g6h2GCsNig3Ml0zZ_nQ130_assertion wasDerivedFrom befree-20140225 NP224329.RAWsckq267gTDqbtHyNpQhg426g6h2GCsNig3Ml0zZ_nQ130_provenance.
- NP224329.RAWsckq267gTDqbtHyNpQhg426g6h2GCsNig3Ml0zZ_nQ130_assertion wasGeneratedBy ECO_0000203 NP224329.RAWsckq267gTDqbtHyNpQhg426g6h2GCsNig3Ml0zZ_nQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP224329.RAWsckq267gTDqbtHyNpQhg426g6h2GCsNig3Ml0zZ_nQ130_provenance.