Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP847585.RALW89zBKxTWFRwx7MDo_u6wQKfllYbqO-Wog5Q1DdrHY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP847585.RALW89zBKxTWFRwx7MDo_u6wQKfllYbqO-Wog5Q1DdrHY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP847585.RALW89zBKxTWFRwx7MDo_u6wQKfllYbqO-Wog5Q1DdrHY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP847585.RALW89zBKxTWFRwx7MDo_u6wQKfllYbqO-Wog5Q1DdrHY130_provenance.
- NP847585.RALW89zBKxTWFRwx7MDo_u6wQKfllYbqO-Wog5Q1DdrHY130_assertion description "[Further combined analysis of ACTA2 and other, possibly causative, genes in larger cohorts of MMD and other vascular diseases may identify possible common disease-causing mechanisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP847585.RALW89zBKxTWFRwx7MDo_u6wQKfllYbqO-Wog5Q1DdrHY130_provenance.
- NP847585.RALW89zBKxTWFRwx7MDo_u6wQKfllYbqO-Wog5Q1DdrHY130_assertion evidence source_evidence_literature NP847585.RALW89zBKxTWFRwx7MDo_u6wQKfllYbqO-Wog5Q1DdrHY130_provenance.
- NP847585.RALW89zBKxTWFRwx7MDo_u6wQKfllYbqO-Wog5Q1DdrHY130_assertion SIO_000772 20970362 NP847585.RALW89zBKxTWFRwx7MDo_u6wQKfllYbqO-Wog5Q1DdrHY130_provenance.
- NP847585.RALW89zBKxTWFRwx7MDo_u6wQKfllYbqO-Wog5Q1DdrHY130_assertion wasDerivedFrom befree-2016 NP847585.RALW89zBKxTWFRwx7MDo_u6wQKfllYbqO-Wog5Q1DdrHY130_provenance.
- NP847585.RALW89zBKxTWFRwx7MDo_u6wQKfllYbqO-Wog5Q1DdrHY130_assertion wasGeneratedBy ECO_0000203 NP847585.RALW89zBKxTWFRwx7MDo_u6wQKfllYbqO-Wog5Q1DdrHY130_provenance.
- befree-2016 importedOn "2016-02-19" NP847585.RALW89zBKxTWFRwx7MDo_u6wQKfllYbqO-Wog5Q1DdrHY130_provenance.