Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP757487.RATur82SVzESkTu83h109X5xBx9Pcm934vckmu4Y-XdVI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP757487.RATur82SVzESkTu83h109X5xBx9Pcm934vckmu4Y-XdVI130_assertion type Assertion NP757487.RATur82SVzESkTu83h109X5xBx9Pcm934vckmu4Y-XdVI130_head.
- NP757487.RATur82SVzESkTu83h109X5xBx9Pcm934vckmu4Y-XdVI130_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." NP757487.RATur82SVzESkTu83h109X5xBx9Pcm934vckmu4Y-XdVI130_provenance.
- NP757487.RATur82SVzESkTu83h109X5xBx9Pcm934vckmu4Y-XdVI130_assertion evidence source_evidence_literature NP757487.RATur82SVzESkTu83h109X5xBx9Pcm934vckmu4Y-XdVI130_provenance.
- NP757487.RATur82SVzESkTu83h109X5xBx9Pcm934vckmu4Y-XdVI130_assertion SIO_000772 16754686 NP757487.RATur82SVzESkTu83h109X5xBx9Pcm934vckmu4Y-XdVI130_provenance.
- NP757487.RATur82SVzESkTu83h109X5xBx9Pcm934vckmu4Y-XdVI130_assertion wasDerivedFrom befree-20140225 NP757487.RATur82SVzESkTu83h109X5xBx9Pcm934vckmu4Y-XdVI130_provenance.
- NP757487.RATur82SVzESkTu83h109X5xBx9Pcm934vckmu4Y-XdVI130_assertion wasGeneratedBy ECO_0000203 NP757487.RATur82SVzESkTu83h109X5xBx9Pcm934vckmu4Y-XdVI130_provenance.