Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP223372.RAkHLoWbhTaoLXcs9rghkm1wsALW-7MEPcHpONBTcVJ_I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP223372.RAkHLoWbhTaoLXcs9rghkm1wsALW-7MEPcHpONBTcVJ_I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP223372.RAkHLoWbhTaoLXcs9rghkm1wsALW-7MEPcHpONBTcVJ_I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP223372.RAkHLoWbhTaoLXcs9rghkm1wsALW-7MEPcHpONBTcVJ_I130_provenance.
- NP223372.RAkHLoWbhTaoLXcs9rghkm1wsALW-7MEPcHpONBTcVJ_I130_assertion description "[Mutations in the CACNA1A calcium channel subunit gene on chromosome 19 are associated with a wide spectrum of mutation-specific episodic and chronic neurological disorders, including FHM with or without coma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP223372.RAkHLoWbhTaoLXcs9rghkm1wsALW-7MEPcHpONBTcVJ_I130_provenance.
- NP223372.RAkHLoWbhTaoLXcs9rghkm1wsALW-7MEPcHpONBTcVJ_I130_assertion evidence source_evidence_literature NP223372.RAkHLoWbhTaoLXcs9rghkm1wsALW-7MEPcHpONBTcVJ_I130_provenance.
- NP223372.RAkHLoWbhTaoLXcs9rghkm1wsALW-7MEPcHpONBTcVJ_I130_assertion SIO_000772 11409427 NP223372.RAkHLoWbhTaoLXcs9rghkm1wsALW-7MEPcHpONBTcVJ_I130_provenance.
- NP223372.RAkHLoWbhTaoLXcs9rghkm1wsALW-7MEPcHpONBTcVJ_I130_assertion wasDerivedFrom befree-20140225 NP223372.RAkHLoWbhTaoLXcs9rghkm1wsALW-7MEPcHpONBTcVJ_I130_provenance.
- NP223372.RAkHLoWbhTaoLXcs9rghkm1wsALW-7MEPcHpONBTcVJ_I130_assertion wasGeneratedBy ECO_0000203 NP223372.RAkHLoWbhTaoLXcs9rghkm1wsALW-7MEPcHpONBTcVJ_I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP223372.RAkHLoWbhTaoLXcs9rghkm1wsALW-7MEPcHpONBTcVJ_I130_provenance.