Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP599606.RAYevkk6RAkGVK1f0hRuG385egN0xGb1a1G6Euq1gq4yk130_assertion> ?p ?o ?g. }
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- NP599606.RAYevkk6RAkGVK1f0hRuG385egN0xGb1a1G6Euq1gq4yk130_assertion type Assertion NP599606.RAYevkk6RAkGVK1f0hRuG385egN0xGb1a1G6Euq1gq4yk130_head.
- NP599606.RAYevkk6RAkGVK1f0hRuG385egN0xGb1a1G6Euq1gq4yk130_assertion description "[Previous studies implicate CACNA1C (L-type Ca(V)1.2) calcium channel mutations in a disorder associated with autism (Timothy syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP599606.RAYevkk6RAkGVK1f0hRuG385egN0xGb1a1G6Euq1gq4yk130_provenance.
- NP599606.RAYevkk6RAkGVK1f0hRuG385egN0xGb1a1G6Euq1gq4yk130_assertion evidence source_evidence_literature NP599606.RAYevkk6RAkGVK1f0hRuG385egN0xGb1a1G6Euq1gq4yk130_provenance.
- NP599606.RAYevkk6RAkGVK1f0hRuG385egN0xGb1a1G6Euq1gq4yk130_assertion SIO_000772 16754686 NP599606.RAYevkk6RAkGVK1f0hRuG385egN0xGb1a1G6Euq1gq4yk130_provenance.
- NP599606.RAYevkk6RAkGVK1f0hRuG385egN0xGb1a1G6Euq1gq4yk130_assertion wasDerivedFrom befree-20140225 NP599606.RAYevkk6RAkGVK1f0hRuG385egN0xGb1a1G6Euq1gq4yk130_provenance.
- NP599606.RAYevkk6RAkGVK1f0hRuG385egN0xGb1a1G6Euq1gq4yk130_assertion wasGeneratedBy ECO_0000203 NP599606.RAYevkk6RAkGVK1f0hRuG385egN0xGb1a1G6Euq1gq4yk130_provenance.