Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP192612.RARc1MXiJepfzeBJyPGXqodloTy7IOO0ENP2RL2k1rMcA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP192612.RARc1MXiJepfzeBJyPGXqodloTy7IOO0ENP2RL2k1rMcA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP192612.RARc1MXiJepfzeBJyPGXqodloTy7IOO0ENP2RL2k1rMcA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP192612.RARc1MXiJepfzeBJyPGXqodloTy7IOO0ENP2RL2k1rMcA130_provenance.
- NP192612.RARc1MXiJepfzeBJyPGXqodloTy7IOO0ENP2RL2k1rMcA130_assertion description "[missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP192612.RARc1MXiJepfzeBJyPGXqodloTy7IOO0ENP2RL2k1rMcA130_provenance.
- NP192612.RARc1MXiJepfzeBJyPGXqodloTy7IOO0ENP2RL2k1rMcA130_assertion evidence source_evidence_literature NP192612.RARc1MXiJepfzeBJyPGXqodloTy7IOO0ENP2RL2k1rMcA130_provenance.
- NP192612.RARc1MXiJepfzeBJyPGXqodloTy7IOO0ENP2RL2k1rMcA130_assertion SIO_000772 11704930 NP192612.RARc1MXiJepfzeBJyPGXqodloTy7IOO0ENP2RL2k1rMcA130_provenance.
- NP192612.RARc1MXiJepfzeBJyPGXqodloTy7IOO0ENP2RL2k1rMcA130_assertion wasDerivedFrom lhgdn-20090331 NP192612.RARc1MXiJepfzeBJyPGXqodloTy7IOO0ENP2RL2k1rMcA130_provenance.
- NP192612.RARc1MXiJepfzeBJyPGXqodloTy7IOO0ENP2RL2k1rMcA130_assertion wasGeneratedBy ECO_0000203 NP192612.RARc1MXiJepfzeBJyPGXqodloTy7IOO0ENP2RL2k1rMcA130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP192612.RARc1MXiJepfzeBJyPGXqodloTy7IOO0ENP2RL2k1rMcA130_provenance.