Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP267903.RAdBTQEl_BhaeSEhPczSgBLCRDdih2vmRSMlmSMi_t1UQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP267903.RAdBTQEl_BhaeSEhPczSgBLCRDdih2vmRSMlmSMi_t1UQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP267903.RAdBTQEl_BhaeSEhPczSgBLCRDdih2vmRSMlmSMi_t1UQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP267903.RAdBTQEl_BhaeSEhPczSgBLCRDdih2vmRSMlmSMi_t1UQ130_provenance.
- NP267903.RAdBTQEl_BhaeSEhPczSgBLCRDdih2vmRSMlmSMi_t1UQ130_assertion description "[Two novel CACNA1A gene mutations associated with episodic ataxia type 2 and interictal dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP267903.RAdBTQEl_BhaeSEhPczSgBLCRDdih2vmRSMlmSMi_t1UQ130_provenance.
- NP267903.RAdBTQEl_BhaeSEhPczSgBLCRDdih2vmRSMlmSMi_t1UQ130_assertion evidence source_evidence_literature NP267903.RAdBTQEl_BhaeSEhPczSgBLCRDdih2vmRSMlmSMi_t1UQ130_provenance.
- NP267903.RAdBTQEl_BhaeSEhPczSgBLCRDdih2vmRSMlmSMi_t1UQ130_assertion SIO_000772 15710862 NP267903.RAdBTQEl_BhaeSEhPczSgBLCRDdih2vmRSMlmSMi_t1UQ130_provenance.
- NP267903.RAdBTQEl_BhaeSEhPczSgBLCRDdih2vmRSMlmSMi_t1UQ130_assertion wasDerivedFrom befree-20140225 NP267903.RAdBTQEl_BhaeSEhPczSgBLCRDdih2vmRSMlmSMi_t1UQ130_provenance.
- NP267903.RAdBTQEl_BhaeSEhPczSgBLCRDdih2vmRSMlmSMi_t1UQ130_assertion wasGeneratedBy ECO_0000203 NP267903.RAdBTQEl_BhaeSEhPczSgBLCRDdih2vmRSMlmSMi_t1UQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP267903.RAdBTQEl_BhaeSEhPczSgBLCRDdih2vmRSMlmSMi_t1UQ130_provenance.