Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP609401.RAYHvFE2QlpkmLicafYwuDhseOjNdKBwpiB8WbgKgjIBE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP609401.RAYHvFE2QlpkmLicafYwuDhseOjNdKBwpiB8WbgKgjIBE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP609401.RAYHvFE2QlpkmLicafYwuDhseOjNdKBwpiB8WbgKgjIBE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP609401.RAYHvFE2QlpkmLicafYwuDhseOjNdKBwpiB8WbgKgjIBE130_provenance.
- NP609401.RAYHvFE2QlpkmLicafYwuDhseOjNdKBwpiB8WbgKgjIBE130_assertion description "[Since no linkage between MYH7 mutation and HCM with WPW syndrome has been reported to date, we cannot conclude whether the observed mutation is a common cause for both diseases, or this patient presents an incidental co-occurrence of HCM (caused by MYH7 mutation) and WPW syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609401.RAYHvFE2QlpkmLicafYwuDhseOjNdKBwpiB8WbgKgjIBE130_provenance.
- NP609401.RAYHvFE2QlpkmLicafYwuDhseOjNdKBwpiB8WbgKgjIBE130_assertion evidence source_evidence_literature NP609401.RAYHvFE2QlpkmLicafYwuDhseOjNdKBwpiB8WbgKgjIBE130_provenance.
- NP609401.RAYHvFE2QlpkmLicafYwuDhseOjNdKBwpiB8WbgKgjIBE130_assertion SIO_000772 17495353 NP609401.RAYHvFE2QlpkmLicafYwuDhseOjNdKBwpiB8WbgKgjIBE130_provenance.
- NP609401.RAYHvFE2QlpkmLicafYwuDhseOjNdKBwpiB8WbgKgjIBE130_assertion wasDerivedFrom befree-2016 NP609401.RAYHvFE2QlpkmLicafYwuDhseOjNdKBwpiB8WbgKgjIBE130_provenance.
- NP609401.RAYHvFE2QlpkmLicafYwuDhseOjNdKBwpiB8WbgKgjIBE130_assertion wasGeneratedBy ECO_0000203 NP609401.RAYHvFE2QlpkmLicafYwuDhseOjNdKBwpiB8WbgKgjIBE130_provenance.
- befree-2016 importedOn "2016-02-19" NP609401.RAYHvFE2QlpkmLicafYwuDhseOjNdKBwpiB8WbgKgjIBE130_provenance.