Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP776610.RAAr8I-J_ykeoGzCGSTS56WTktumjkuC1_IqkD_LEKKA0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP776610.RAAr8I-J_ykeoGzCGSTS56WTktumjkuC1_IqkD_LEKKA0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP776610.RAAr8I-J_ykeoGzCGSTS56WTktumjkuC1_IqkD_LEKKA0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP776610.RAAr8I-J_ykeoGzCGSTS56WTktumjkuC1_IqkD_LEKKA0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP776610.RAAr8I-J_ykeoGzCGSTS56WTktumjkuC1_IqkD_LEKKA0130_provenance.
- NP776610.RAAr8I-J_ykeoGzCGSTS56WTktumjkuC1_IqkD_LEKKA0130_assertion wasGeneratedBy ECO_0000203 NP776610.RAAr8I-J_ykeoGzCGSTS56WTktumjkuC1_IqkD_LEKKA0130_provenance.
- NP776610.RAAr8I-J_ykeoGzCGSTS56WTktumjkuC1_IqkD_LEKKA0130_assertion wasDerivedFrom befree-20150227 NP776610.RAAr8I-J_ykeoGzCGSTS56WTktumjkuC1_IqkD_LEKKA0130_provenance.
- NP776610.RAAr8I-J_ykeoGzCGSTS56WTktumjkuC1_IqkD_LEKKA0130_assertion SIO_000772 10570326 NP776610.RAAr8I-J_ykeoGzCGSTS56WTktumjkuC1_IqkD_LEKKA0130_provenance.
- NP776610.RAAr8I-J_ykeoGzCGSTS56WTktumjkuC1_IqkD_LEKKA0130_assertion evidence source_evidence_literature NP776610.RAAr8I-J_ykeoGzCGSTS56WTktumjkuC1_IqkD_LEKKA0130_provenance.
- NP776610.RAAr8I-J_ykeoGzCGSTS56WTktumjkuC1_IqkD_LEKKA0130_assertion description "[Wiskott-Aldrich syndrome, an inherited blood cell disorder due to mutations of the X-chromosome gene WASP (Wiskott-Aldrich syndrome protein), was characterized originally by thrombocytopenia, immunodeficiency, and eczema.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776610.RAAr8I-J_ykeoGzCGSTS56WTktumjkuC1_IqkD_LEKKA0130_provenance.