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- source_evidence_literature type ECO_0000212 NP209946.RAkMo6B248oQCJSxjAypma4mZnqis5sFocAV-rh3tjuao130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP209946.RAkMo6B248oQCJSxjAypma4mZnqis5sFocAV-rh3tjuao130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP209946.RAkMo6B248oQCJSxjAypma4mZnqis5sFocAV-rh3tjuao130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP209946.RAkMo6B248oQCJSxjAypma4mZnqis5sFocAV-rh3tjuao130_provenance.
- NP209946.RAkMo6B248oQCJSxjAypma4mZnqis5sFocAV-rh3tjuao130_assertion wasGeneratedBy ECO_0000203 NP209946.RAkMo6B248oQCJSxjAypma4mZnqis5sFocAV-rh3tjuao130_provenance.
- NP209946.RAkMo6B248oQCJSxjAypma4mZnqis5sFocAV-rh3tjuao130_assertion wasDerivedFrom lhgdn-20090331 NP209946.RAkMo6B248oQCJSxjAypma4mZnqis5sFocAV-rh3tjuao130_provenance.
- NP209946.RAkMo6B248oQCJSxjAypma4mZnqis5sFocAV-rh3tjuao130_assertion SIO_000772 17400488 NP209946.RAkMo6B248oQCJSxjAypma4mZnqis5sFocAV-rh3tjuao130_provenance.
- NP209946.RAkMo6B248oQCJSxjAypma4mZnqis5sFocAV-rh3tjuao130_assertion evidence source_evidence_literature NP209946.RAkMo6B248oQCJSxjAypma4mZnqis5sFocAV-rh3tjuao130_provenance.
- NP209946.RAkMo6B248oQCJSxjAypma4mZnqis5sFocAV-rh3tjuao130_assertion description "[study found 28 novel WAS mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia (7 missense, 1 nonsense, 1 nonstop change, 5 splice site mutations and 14 deletions or insertions) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209946.RAkMo6B248oQCJSxjAypma4mZnqis5sFocAV-rh3tjuao130_provenance.