Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_provenance.
- NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_assertion description "[Two genes have been identified for the X-linked forms (dystrophin and tafazzin), whereas three other genes (actin, lamin A/C, and desmin) cause autosomal dominant DCM; seven other loci for autosomal dominant DCM have been mapped but the genes have not been identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_provenance.
- NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_assertion evidence source_evidence_literature NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_provenance.
- NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_assertion SIO_000772 10974018 NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_provenance.
- NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_assertion wasDerivedFrom befree-2016 NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_provenance.
- NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_assertion wasGeneratedBy ECO_0000203 NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_provenance.
- befree-2016 importedOn "2016-02-19" NP294218.RAaE1yF7d9IsvauIiIglU3BUAdhHrQdwEILT5MpzoT7-o130_provenance.