Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP830619.RAxl0FxjsbZWaGQNr33zVvGEXJ82pfvIHLM-E0oCreAr0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP830619.RAxl0FxjsbZWaGQNr33zVvGEXJ82pfvIHLM-E0oCreAr0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP830619.RAxl0FxjsbZWaGQNr33zVvGEXJ82pfvIHLM-E0oCreAr0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP830619.RAxl0FxjsbZWaGQNr33zVvGEXJ82pfvIHLM-E0oCreAr0130_provenance.
- NP830619.RAxl0FxjsbZWaGQNr33zVvGEXJ82pfvIHLM-E0oCreAr0130_assertion description "[Based upon these data, and the recent descriptions of mutations in MLP in patients with DCM or hypertrophic cardiomyopathy, we screened patients for mutations in the MLP and alpha-actinin-2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP830619.RAxl0FxjsbZWaGQNr33zVvGEXJ82pfvIHLM-E0oCreAr0130_provenance.
- NP830619.RAxl0FxjsbZWaGQNr33zVvGEXJ82pfvIHLM-E0oCreAr0130_assertion evidence source_evidence_literature NP830619.RAxl0FxjsbZWaGQNr33zVvGEXJ82pfvIHLM-E0oCreAr0130_provenance.
- NP830619.RAxl0FxjsbZWaGQNr33zVvGEXJ82pfvIHLM-E0oCreAr0130_assertion SIO_000772 14567970 NP830619.RAxl0FxjsbZWaGQNr33zVvGEXJ82pfvIHLM-E0oCreAr0130_provenance.
- NP830619.RAxl0FxjsbZWaGQNr33zVvGEXJ82pfvIHLM-E0oCreAr0130_assertion wasDerivedFrom befree-20140225 NP830619.RAxl0FxjsbZWaGQNr33zVvGEXJ82pfvIHLM-E0oCreAr0130_provenance.
- NP830619.RAxl0FxjsbZWaGQNr33zVvGEXJ82pfvIHLM-E0oCreAr0130_assertion wasGeneratedBy ECO_0000203 NP830619.RAxl0FxjsbZWaGQNr33zVvGEXJ82pfvIHLM-E0oCreAr0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP830619.RAxl0FxjsbZWaGQNr33zVvGEXJ82pfvIHLM-E0oCreAr0130_provenance.