Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP511675.RA6TTgwXj32Jbe8z0-jCZsfdlFdgYBslgXJzK62i_K-IA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP511675.RA6TTgwXj32Jbe8z0-jCZsfdlFdgYBslgXJzK62i_K-IA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP511675.RA6TTgwXj32Jbe8z0-jCZsfdlFdgYBslgXJzK62i_K-IA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP511675.RA6TTgwXj32Jbe8z0-jCZsfdlFdgYBslgXJzK62i_K-IA130_provenance.
- NP511675.RA6TTgwXj32Jbe8z0-jCZsfdlFdgYBslgXJzK62i_K-IA130_assertion description "[Fatal hypertrophic cardiomyopathy and nemaline myopathy associated with ACTA1 K336E mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP511675.RA6TTgwXj32Jbe8z0-jCZsfdlFdgYBslgXJzK62i_K-IA130_provenance.
- NP511675.RA6TTgwXj32Jbe8z0-jCZsfdlFdgYBslgXJzK62i_K-IA130_assertion evidence source_evidence_literature NP511675.RA6TTgwXj32Jbe8z0-jCZsfdlFdgYBslgXJzK62i_K-IA130_provenance.
- NP511675.RA6TTgwXj32Jbe8z0-jCZsfdlFdgYBslgXJzK62i_K-IA130_assertion SIO_000772 16945537 NP511675.RA6TTgwXj32Jbe8z0-jCZsfdlFdgYBslgXJzK62i_K-IA130_provenance.
- NP511675.RA6TTgwXj32Jbe8z0-jCZsfdlFdgYBslgXJzK62i_K-IA130_assertion wasDerivedFrom befree-20140225 NP511675.RA6TTgwXj32Jbe8z0-jCZsfdlFdgYBslgXJzK62i_K-IA130_provenance.
- NP511675.RA6TTgwXj32Jbe8z0-jCZsfdlFdgYBslgXJzK62i_K-IA130_assertion wasGeneratedBy ECO_0000203 NP511675.RA6TTgwXj32Jbe8z0-jCZsfdlFdgYBslgXJzK62i_K-IA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP511675.RA6TTgwXj32Jbe8z0-jCZsfdlFdgYBslgXJzK62i_K-IA130_provenance.