Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP134982.RAd9z_F7JZWNdY2VNmPu3cePJ8RU1X9MUa1jgwHtvPEjU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP134982.RAd9z_F7JZWNdY2VNmPu3cePJ8RU1X9MUa1jgwHtvPEjU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP134982.RAd9z_F7JZWNdY2VNmPu3cePJ8RU1X9MUa1jgwHtvPEjU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP134982.RAd9z_F7JZWNdY2VNmPu3cePJ8RU1X9MUa1jgwHtvPEjU130_provenance.
- NP134982.RAd9z_F7JZWNdY2VNmPu3cePJ8RU1X9MUa1jgwHtvPEjU130_assertion description "[Missense mutations of ACTA1 cause an autosomal dominant congenital myopathy with cores.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP134982.RAd9z_F7JZWNdY2VNmPu3cePJ8RU1X9MUa1jgwHtvPEjU130_provenance.
- NP134982.RAd9z_F7JZWNdY2VNmPu3cePJ8RU1X9MUa1jgwHtvPEjU130_assertion evidence source_evidence_literature NP134982.RAd9z_F7JZWNdY2VNmPu3cePJ8RU1X9MUa1jgwHtvPEjU130_provenance.
- NP134982.RAd9z_F7JZWNdY2VNmPu3cePJ8RU1X9MUa1jgwHtvPEjU130_assertion SIO_000772 15520409 NP134982.RAd9z_F7JZWNdY2VNmPu3cePJ8RU1X9MUa1jgwHtvPEjU130_provenance.
- NP134982.RAd9z_F7JZWNdY2VNmPu3cePJ8RU1X9MUa1jgwHtvPEjU130_assertion wasDerivedFrom lhgdn-20090331 NP134982.RAd9z_F7JZWNdY2VNmPu3cePJ8RU1X9MUa1jgwHtvPEjU130_provenance.
- NP134982.RAd9z_F7JZWNdY2VNmPu3cePJ8RU1X9MUa1jgwHtvPEjU130_assertion wasGeneratedBy ECO_0000203 NP134982.RAd9z_F7JZWNdY2VNmPu3cePJ8RU1X9MUa1jgwHtvPEjU130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP134982.RAd9z_F7JZWNdY2VNmPu3cePJ8RU1X9MUa1jgwHtvPEjU130_provenance.