Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP694700.RASRgWyTF-3bH7KoWCzl_hmvZZiBPicG7jLlX2QBID2Tc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP694700.RASRgWyTF-3bH7KoWCzl_hmvZZiBPicG7jLlX2QBID2Tc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP694700.RASRgWyTF-3bH7KoWCzl_hmvZZiBPicG7jLlX2QBID2Tc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP694700.RASRgWyTF-3bH7KoWCzl_hmvZZiBPicG7jLlX2QBID2Tc130_provenance.
- NP694700.RASRgWyTF-3bH7KoWCzl_hmvZZiBPicG7jLlX2QBID2Tc130_assertion description "[The seven missense mutations reported to date occur only within the ubiquitin (Ub)-specific protease (USP) domain of the CYLD protein and most are associated exclusively with multiple familial trichoepithelioma (MFT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694700.RASRgWyTF-3bH7KoWCzl_hmvZZiBPicG7jLlX2QBID2Tc130_provenance.
- NP694700.RASRgWyTF-3bH7KoWCzl_hmvZZiBPicG7jLlX2QBID2Tc130_assertion evidence source_evidence_literature NP694700.RASRgWyTF-3bH7KoWCzl_hmvZZiBPicG7jLlX2QBID2Tc130_provenance.
- NP694700.RASRgWyTF-3bH7KoWCzl_hmvZZiBPicG7jLlX2QBID2Tc130_assertion SIO_000772 19462465 NP694700.RASRgWyTF-3bH7KoWCzl_hmvZZiBPicG7jLlX2QBID2Tc130_provenance.
- NP694700.RASRgWyTF-3bH7KoWCzl_hmvZZiBPicG7jLlX2QBID2Tc130_assertion wasDerivedFrom befree-20140225 NP694700.RASRgWyTF-3bH7KoWCzl_hmvZZiBPicG7jLlX2QBID2Tc130_provenance.
- NP694700.RASRgWyTF-3bH7KoWCzl_hmvZZiBPicG7jLlX2QBID2Tc130_assertion wasGeneratedBy ECO_0000203 NP694700.RASRgWyTF-3bH7KoWCzl_hmvZZiBPicG7jLlX2QBID2Tc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP694700.RASRgWyTF-3bH7KoWCzl_hmvZZiBPicG7jLlX2QBID2Tc130_provenance.