Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP846481.RAod4PYhD-suEXbS7xQjEpR61ElR1Oe6TOvPZqH6uKtrc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP846481.RAod4PYhD-suEXbS7xQjEpR61ElR1Oe6TOvPZqH6uKtrc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP846481.RAod4PYhD-suEXbS7xQjEpR61ElR1Oe6TOvPZqH6uKtrc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP846481.RAod4PYhD-suEXbS7xQjEpR61ElR1Oe6TOvPZqH6uKtrc130_provenance.
- NP846481.RAod4PYhD-suEXbS7xQjEpR61ElR1Oe6TOvPZqH6uKtrc130_assertion description "[Previous studies implicate CACNA1C (L-type Ca(V)1.2) calcium channel mutations in a disorder associated with autism (Timothy syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP846481.RAod4PYhD-suEXbS7xQjEpR61ElR1Oe6TOvPZqH6uKtrc130_provenance.
- NP846481.RAod4PYhD-suEXbS7xQjEpR61ElR1Oe6TOvPZqH6uKtrc130_assertion evidence source_evidence_literature NP846481.RAod4PYhD-suEXbS7xQjEpR61ElR1Oe6TOvPZqH6uKtrc130_provenance.
- NP846481.RAod4PYhD-suEXbS7xQjEpR61ElR1Oe6TOvPZqH6uKtrc130_assertion SIO_000772 16754686 NP846481.RAod4PYhD-suEXbS7xQjEpR61ElR1Oe6TOvPZqH6uKtrc130_provenance.
- NP846481.RAod4PYhD-suEXbS7xQjEpR61ElR1Oe6TOvPZqH6uKtrc130_assertion wasDerivedFrom befree-20140225 NP846481.RAod4PYhD-suEXbS7xQjEpR61ElR1Oe6TOvPZqH6uKtrc130_provenance.
- NP846481.RAod4PYhD-suEXbS7xQjEpR61ElR1Oe6TOvPZqH6uKtrc130_assertion wasGeneratedBy ECO_0000203 NP846481.RAod4PYhD-suEXbS7xQjEpR61ElR1Oe6TOvPZqH6uKtrc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP846481.RAod4PYhD-suEXbS7xQjEpR61ElR1Oe6TOvPZqH6uKtrc130_provenance.