Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP276942.RAdEUP1KuIwrCFipq-FuRex8RGOQwB2Ia_TseW3nAqxZg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP276942.RAdEUP1KuIwrCFipq-FuRex8RGOQwB2Ia_TseW3nAqxZg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP276942.RAdEUP1KuIwrCFipq-FuRex8RGOQwB2Ia_TseW3nAqxZg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP276942.RAdEUP1KuIwrCFipq-FuRex8RGOQwB2Ia_TseW3nAqxZg130_provenance.
- NP276942.RAdEUP1KuIwrCFipq-FuRex8RGOQwB2Ia_TseW3nAqxZg130_assertion description "[Familial hemiplegic migraine is caused by CACNA1A missense mutations in 50% of families, including all families with cerebellar ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276942.RAdEUP1KuIwrCFipq-FuRex8RGOQwB2Ia_TseW3nAqxZg130_provenance.
- NP276942.RAdEUP1KuIwrCFipq-FuRex8RGOQwB2Ia_TseW3nAqxZg130_assertion evidence source_evidence_literature NP276942.RAdEUP1KuIwrCFipq-FuRex8RGOQwB2Ia_TseW3nAqxZg130_provenance.
- NP276942.RAdEUP1KuIwrCFipq-FuRex8RGOQwB2Ia_TseW3nAqxZg130_assertion SIO_000772 11061267 NP276942.RAdEUP1KuIwrCFipq-FuRex8RGOQwB2Ia_TseW3nAqxZg130_provenance.
- NP276942.RAdEUP1KuIwrCFipq-FuRex8RGOQwB2Ia_TseW3nAqxZg130_assertion wasDerivedFrom befree-20150227 NP276942.RAdEUP1KuIwrCFipq-FuRex8RGOQwB2Ia_TseW3nAqxZg130_provenance.
- NP276942.RAdEUP1KuIwrCFipq-FuRex8RGOQwB2Ia_TseW3nAqxZg130_assertion wasGeneratedBy ECO_0000203 NP276942.RAdEUP1KuIwrCFipq-FuRex8RGOQwB2Ia_TseW3nAqxZg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP276942.RAdEUP1KuIwrCFipq-FuRex8RGOQwB2Ia_TseW3nAqxZg130_provenance.