Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1247408.RAud1B6ax98ogeFYaX15oP4lU37vUq317Vpq1_RH1AHQA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1247408.RAud1B6ax98ogeFYaX15oP4lU37vUq317Vpq1_RH1AHQA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1247408.RAud1B6ax98ogeFYaX15oP4lU37vUq317Vpq1_RH1AHQA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1247408.RAud1B6ax98ogeFYaX15oP4lU37vUq317Vpq1_RH1AHQA130_provenance.
- NP1247408.RAud1B6ax98ogeFYaX15oP4lU37vUq317Vpq1_RH1AHQA130_assertion description "[This large-animal model exhibits many phenotypes seen in patients with SCN5A loss-of-function mutations and has the potential to provide important insight into sodium channelopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1247408.RAud1B6ax98ogeFYaX15oP4lU37vUq317Vpq1_RH1AHQA130_provenance.
- NP1247408.RAud1B6ax98ogeFYaX15oP4lU37vUq317Vpq1_RH1AHQA130_assertion evidence source_evidence_literature NP1247408.RAud1B6ax98ogeFYaX15oP4lU37vUq317Vpq1_RH1AHQA130_provenance.
- NP1247408.RAud1B6ax98ogeFYaX15oP4lU37vUq317Vpq1_RH1AHQA130_assertion SIO_000772 25500878 NP1247408.RAud1B6ax98ogeFYaX15oP4lU37vUq317Vpq1_RH1AHQA130_provenance.
- NP1247408.RAud1B6ax98ogeFYaX15oP4lU37vUq317Vpq1_RH1AHQA130_assertion wasDerivedFrom befree-2016 NP1247408.RAud1B6ax98ogeFYaX15oP4lU37vUq317Vpq1_RH1AHQA130_provenance.
- NP1247408.RAud1B6ax98ogeFYaX15oP4lU37vUq317Vpq1_RH1AHQA130_assertion wasGeneratedBy ECO_0000203 NP1247408.RAud1B6ax98ogeFYaX15oP4lU37vUq317Vpq1_RH1AHQA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1247408.RAud1B6ax98ogeFYaX15oP4lU37vUq317Vpq1_RH1AHQA130_provenance.