Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP553185.RAFYfvSH_BY60loJyd1ErLl_6o43VCQg31n0dnPEs6vVo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP553185.RAFYfvSH_BY60loJyd1ErLl_6o43VCQg31n0dnPEs6vVo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP553185.RAFYfvSH_BY60loJyd1ErLl_6o43VCQg31n0dnPEs6vVo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP553185.RAFYfvSH_BY60loJyd1ErLl_6o43VCQg31n0dnPEs6vVo130_provenance.
- NP553185.RAFYfvSH_BY60loJyd1ErLl_6o43VCQg31n0dnPEs6vVo130_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." NP553185.RAFYfvSH_BY60loJyd1ErLl_6o43VCQg31n0dnPEs6vVo130_provenance.
- NP553185.RAFYfvSH_BY60loJyd1ErLl_6o43VCQg31n0dnPEs6vVo130_assertion evidence source_evidence_literature NP553185.RAFYfvSH_BY60loJyd1ErLl_6o43VCQg31n0dnPEs6vVo130_provenance.
- NP553185.RAFYfvSH_BY60loJyd1ErLl_6o43VCQg31n0dnPEs6vVo130_assertion SIO_000772 16754686 NP553185.RAFYfvSH_BY60loJyd1ErLl_6o43VCQg31n0dnPEs6vVo130_provenance.
- NP553185.RAFYfvSH_BY60loJyd1ErLl_6o43VCQg31n0dnPEs6vVo130_assertion wasDerivedFrom befree-2016 NP553185.RAFYfvSH_BY60loJyd1ErLl_6o43VCQg31n0dnPEs6vVo130_provenance.
- NP553185.RAFYfvSH_BY60loJyd1ErLl_6o43VCQg31n0dnPEs6vVo130_assertion wasGeneratedBy ECO_0000203 NP553185.RAFYfvSH_BY60loJyd1ErLl_6o43VCQg31n0dnPEs6vVo130_provenance.
- befree-2016 importedOn "2016-02-19" NP553185.RAFYfvSH_BY60loJyd1ErLl_6o43VCQg31n0dnPEs6vVo130_provenance.