Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP308198.RAXJ5WeQxj6Tbs-pwp9bYvW81zPljTwfzJC-RFB7o8XvU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP308198.RAXJ5WeQxj6Tbs-pwp9bYvW81zPljTwfzJC-RFB7o8XvU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP308198.RAXJ5WeQxj6Tbs-pwp9bYvW81zPljTwfzJC-RFB7o8XvU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP308198.RAXJ5WeQxj6Tbs-pwp9bYvW81zPljTwfzJC-RFB7o8XvU130_provenance.
- NP308198.RAXJ5WeQxj6Tbs-pwp9bYvW81zPljTwfzJC-RFB7o8XvU130_assertion description "[Mutations have been identified in alpha-tropomyosin (Tm), a key regulatory protein in striated muscle cells, that are associated with a human cardiac myopathy, hypertrophic cardiomyopathy (FHC) and a human skeletal myopathy, nemaline myopathy (NM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP308198.RAXJ5WeQxj6Tbs-pwp9bYvW81zPljTwfzJC-RFB7o8XvU130_provenance.
- NP308198.RAXJ5WeQxj6Tbs-pwp9bYvW81zPljTwfzJC-RFB7o8XvU130_assertion evidence source_evidence_literature NP308198.RAXJ5WeQxj6Tbs-pwp9bYvW81zPljTwfzJC-RFB7o8XvU130_provenance.
- NP308198.RAXJ5WeQxj6Tbs-pwp9bYvW81zPljTwfzJC-RFB7o8XvU130_assertion SIO_000772 11199327 NP308198.RAXJ5WeQxj6Tbs-pwp9bYvW81zPljTwfzJC-RFB7o8XvU130_provenance.
- NP308198.RAXJ5WeQxj6Tbs-pwp9bYvW81zPljTwfzJC-RFB7o8XvU130_assertion wasDerivedFrom befree-2016 NP308198.RAXJ5WeQxj6Tbs-pwp9bYvW81zPljTwfzJC-RFB7o8XvU130_provenance.
- NP308198.RAXJ5WeQxj6Tbs-pwp9bYvW81zPljTwfzJC-RFB7o8XvU130_assertion wasGeneratedBy ECO_0000203 NP308198.RAXJ5WeQxj6Tbs-pwp9bYvW81zPljTwfzJC-RFB7o8XvU130_provenance.
- befree-2016 importedOn "2016-02-19" NP308198.RAXJ5WeQxj6Tbs-pwp9bYvW81zPljTwfzJC-RFB7o8XvU130_provenance.