Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP676925.RA3xG8iAJTaE087x706OBKZeQNsOwqipSaPKtgOFwOFnU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP676925.RA3xG8iAJTaE087x706OBKZeQNsOwqipSaPKtgOFwOFnU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP676925.RA3xG8iAJTaE087x706OBKZeQNsOwqipSaPKtgOFwOFnU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP676925.RA3xG8iAJTaE087x706OBKZeQNsOwqipSaPKtgOFwOFnU130_provenance.
- NP676925.RA3xG8iAJTaE087x706OBKZeQNsOwqipSaPKtgOFwOFnU130_assertion description "[Type I myotonic dystrophy (DM1) is caused by a triplet repeat expansion in the 3'-untranslated region (UTR) of the dystrophia myotonia protein kinase (DMPK) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP676925.RA3xG8iAJTaE087x706OBKZeQNsOwqipSaPKtgOFwOFnU130_provenance.
- NP676925.RA3xG8iAJTaE087x706OBKZeQNsOwqipSaPKtgOFwOFnU130_assertion evidence source_evidence_literature NP676925.RA3xG8iAJTaE087x706OBKZeQNsOwqipSaPKtgOFwOFnU130_provenance.
- NP676925.RA3xG8iAJTaE087x706OBKZeQNsOwqipSaPKtgOFwOFnU130_assertion SIO_000772 18559347 NP676925.RA3xG8iAJTaE087x706OBKZeQNsOwqipSaPKtgOFwOFnU130_provenance.
- NP676925.RA3xG8iAJTaE087x706OBKZeQNsOwqipSaPKtgOFwOFnU130_assertion wasDerivedFrom befree-2016 NP676925.RA3xG8iAJTaE087x706OBKZeQNsOwqipSaPKtgOFwOFnU130_provenance.
- NP676925.RA3xG8iAJTaE087x706OBKZeQNsOwqipSaPKtgOFwOFnU130_assertion wasGeneratedBy ECO_0000203 NP676925.RA3xG8iAJTaE087x706OBKZeQNsOwqipSaPKtgOFwOFnU130_provenance.
- befree-2016 importedOn "2016-02-19" NP676925.RA3xG8iAJTaE087x706OBKZeQNsOwqipSaPKtgOFwOFnU130_provenance.