Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP787174.RAWeOFClgFhN4H1kExlnZWKBgMDKGY0AVyOxWDU9Jpw1c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP787174.RAWeOFClgFhN4H1kExlnZWKBgMDKGY0AVyOxWDU9Jpw1c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP787174.RAWeOFClgFhN4H1kExlnZWKBgMDKGY0AVyOxWDU9Jpw1c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP787174.RAWeOFClgFhN4H1kExlnZWKBgMDKGY0AVyOxWDU9Jpw1c130_provenance.
- NP787174.RAWeOFClgFhN4H1kExlnZWKBgMDKGY0AVyOxWDU9Jpw1c130_assertion description "[Mosaic deletion of Pkd1 resulted in PKD and replicated characteristic features of human PKD including aberrant mTOR activation, epithelial proliferation and apoptosis, and progressive fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787174.RAWeOFClgFhN4H1kExlnZWKBgMDKGY0AVyOxWDU9Jpw1c130_provenance.
- NP787174.RAWeOFClgFhN4H1kExlnZWKBgMDKGY0AVyOxWDU9Jpw1c130_assertion evidence source_evidence_literature NP787174.RAWeOFClgFhN4H1kExlnZWKBgMDKGY0AVyOxWDU9Jpw1c130_provenance.
- NP787174.RAWeOFClgFhN4H1kExlnZWKBgMDKGY0AVyOxWDU9Jpw1c130_assertion SIO_000772 20075061 NP787174.RAWeOFClgFhN4H1kExlnZWKBgMDKGY0AVyOxWDU9Jpw1c130_provenance.
- NP787174.RAWeOFClgFhN4H1kExlnZWKBgMDKGY0AVyOxWDU9Jpw1c130_assertion wasDerivedFrom befree-2016 NP787174.RAWeOFClgFhN4H1kExlnZWKBgMDKGY0AVyOxWDU9Jpw1c130_provenance.
- NP787174.RAWeOFClgFhN4H1kExlnZWKBgMDKGY0AVyOxWDU9Jpw1c130_assertion wasGeneratedBy ECO_0000203 NP787174.RAWeOFClgFhN4H1kExlnZWKBgMDKGY0AVyOxWDU9Jpw1c130_provenance.
- befree-2016 importedOn "2016-02-19" NP787174.RAWeOFClgFhN4H1kExlnZWKBgMDKGY0AVyOxWDU9Jpw1c130_provenance.