Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP321103.RA3kQfglGw79g-Z8CUJUSJxTVqBkYcd0iWrrpHbB1sJxE130_assertion> ?p ?o ?g. }
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- NP321103.RA3kQfglGw79g-Z8CUJUSJxTVqBkYcd0iWrrpHbB1sJxE130_assertion type Assertion NP321103.RA3kQfglGw79g-Z8CUJUSJxTVqBkYcd0iWrrpHbB1sJxE130_head.
- NP321103.RA3kQfglGw79g-Z8CUJUSJxTVqBkYcd0iWrrpHbB1sJxE130_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." NP321103.RA3kQfglGw79g-Z8CUJUSJxTVqBkYcd0iWrrpHbB1sJxE130_provenance.
- NP321103.RA3kQfglGw79g-Z8CUJUSJxTVqBkYcd0iWrrpHbB1sJxE130_assertion evidence source_evidence_literature NP321103.RA3kQfglGw79g-Z8CUJUSJxTVqBkYcd0iWrrpHbB1sJxE130_provenance.
- NP321103.RA3kQfglGw79g-Z8CUJUSJxTVqBkYcd0iWrrpHbB1sJxE130_assertion SIO_000772 11409427 NP321103.RA3kQfglGw79g-Z8CUJUSJxTVqBkYcd0iWrrpHbB1sJxE130_provenance.
- NP321103.RA3kQfglGw79g-Z8CUJUSJxTVqBkYcd0iWrrpHbB1sJxE130_assertion wasDerivedFrom befree-2016 NP321103.RA3kQfglGw79g-Z8CUJUSJxTVqBkYcd0iWrrpHbB1sJxE130_provenance.
- NP321103.RA3kQfglGw79g-Z8CUJUSJxTVqBkYcd0iWrrpHbB1sJxE130_assertion wasGeneratedBy ECO_0000203 NP321103.RA3kQfglGw79g-Z8CUJUSJxTVqBkYcd0iWrrpHbB1sJxE130_provenance.