Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP143709.RA7nlnBQqj42zWHVVW0XKFCktf80fHyrsmD4GaXw5lClI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP143709.RA7nlnBQqj42zWHVVW0XKFCktf80fHyrsmD4GaXw5lClI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP143709.RA7nlnBQqj42zWHVVW0XKFCktf80fHyrsmD4GaXw5lClI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP143709.RA7nlnBQqj42zWHVVW0XKFCktf80fHyrsmD4GaXw5lClI130_provenance.
- NP143709.RA7nlnBQqj42zWHVVW0XKFCktf80fHyrsmD4GaXw5lClI130_assertion description "[missense mutation in the CASQ2 gene is associated with autosomal-recessive CPVT (catecholamine-induced polymorphic ventricular tachycardia).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP143709.RA7nlnBQqj42zWHVVW0XKFCktf80fHyrsmD4GaXw5lClI130_provenance.
- NP143709.RA7nlnBQqj42zWHVVW0XKFCktf80fHyrsmD4GaXw5lClI130_assertion evidence source_evidence_literature NP143709.RA7nlnBQqj42zWHVVW0XKFCktf80fHyrsmD4GaXw5lClI130_provenance.
- NP143709.RA7nlnBQqj42zWHVVW0XKFCktf80fHyrsmD4GaXw5lClI130_assertion SIO_000772 12732448 NP143709.RA7nlnBQqj42zWHVVW0XKFCktf80fHyrsmD4GaXw5lClI130_provenance.
- NP143709.RA7nlnBQqj42zWHVVW0XKFCktf80fHyrsmD4GaXw5lClI130_assertion wasDerivedFrom lhgdn-20090331 NP143709.RA7nlnBQqj42zWHVVW0XKFCktf80fHyrsmD4GaXw5lClI130_provenance.
- NP143709.RA7nlnBQqj42zWHVVW0XKFCktf80fHyrsmD4GaXw5lClI130_assertion wasGeneratedBy ECO_0000203 NP143709.RA7nlnBQqj42zWHVVW0XKFCktf80fHyrsmD4GaXw5lClI130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP143709.RA7nlnBQqj42zWHVVW0XKFCktf80fHyrsmD4GaXw5lClI130_provenance.