Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP889655.RAAzuTj68lah6QAjWiwXqZt_8zyypm3dgXagcv2I-McXE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP889655.RAAzuTj68lah6QAjWiwXqZt_8zyypm3dgXagcv2I-McXE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP889655.RAAzuTj68lah6QAjWiwXqZt_8zyypm3dgXagcv2I-McXE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP889655.RAAzuTj68lah6QAjWiwXqZt_8zyypm3dgXagcv2I-McXE130_provenance.
- NP889655.RAAzuTj68lah6QAjWiwXqZt_8zyypm3dgXagcv2I-McXE130_assertion description "[Although TBMN is an autosomal dominant disease (COL4A3 and COL4A4), ATS can be inherited X-linked (COL4A5), autosomal recessive, or autosomal dominant (both COL4A3 and COL4A4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889655.RAAzuTj68lah6QAjWiwXqZt_8zyypm3dgXagcv2I-McXE130_provenance.
- NP889655.RAAzuTj68lah6QAjWiwXqZt_8zyypm3dgXagcv2I-McXE130_assertion evidence source_evidence_literature NP889655.RAAzuTj68lah6QAjWiwXqZt_8zyypm3dgXagcv2I-McXE130_provenance.
- NP889655.RAAzuTj68lah6QAjWiwXqZt_8zyypm3dgXagcv2I-McXE130_assertion SIO_000772 20177710 NP889655.RAAzuTj68lah6QAjWiwXqZt_8zyypm3dgXagcv2I-McXE130_provenance.
- NP889655.RAAzuTj68lah6QAjWiwXqZt_8zyypm3dgXagcv2I-McXE130_assertion wasDerivedFrom befree-20140225 NP889655.RAAzuTj68lah6QAjWiwXqZt_8zyypm3dgXagcv2I-McXE130_provenance.
- NP889655.RAAzuTj68lah6QAjWiwXqZt_8zyypm3dgXagcv2I-McXE130_assertion wasGeneratedBy ECO_0000203 NP889655.RAAzuTj68lah6QAjWiwXqZt_8zyypm3dgXagcv2I-McXE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP889655.RAAzuTj68lah6QAjWiwXqZt_8zyypm3dgXagcv2I-McXE130_provenance.