Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP223372.RAkHLoWbhTaoLXcs9rghkm1wsALW-7MEPcHpONBTcVJ_I130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP223372.RAkHLoWbhTaoLXcs9rghkm1wsALW-7MEPcHpONBTcVJ_I130_assertion type Assertion NP223372.RAkHLoWbhTaoLXcs9rghkm1wsALW-7MEPcHpONBTcVJ_I130_head.
- 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.