Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP396008.RAnoSWFJSSQP7XoK25I_wb108ZCXtWU9BiG7Huxr2yB_U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP396008.RAnoSWFJSSQP7XoK25I_wb108ZCXtWU9BiG7Huxr2yB_U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP396008.RAnoSWFJSSQP7XoK25I_wb108ZCXtWU9BiG7Huxr2yB_U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP396008.RAnoSWFJSSQP7XoK25I_wb108ZCXtWU9BiG7Huxr2yB_U130_provenance.
- NP396008.RAnoSWFJSSQP7XoK25I_wb108ZCXtWU9BiG7Huxr2yB_U130_assertion wasGeneratedBy ECO_0000203 NP396008.RAnoSWFJSSQP7XoK25I_wb108ZCXtWU9BiG7Huxr2yB_U130_provenance.
- NP396008.RAnoSWFJSSQP7XoK25I_wb108ZCXtWU9BiG7Huxr2yB_U130_assertion wasDerivedFrom befree-20140225 NP396008.RAnoSWFJSSQP7XoK25I_wb108ZCXtWU9BiG7Huxr2yB_U130_provenance.
- NP396008.RAnoSWFJSSQP7XoK25I_wb108ZCXtWU9BiG7Huxr2yB_U130_assertion SIO_000772 15761194 NP396008.RAnoSWFJSSQP7XoK25I_wb108ZCXtWU9BiG7Huxr2yB_U130_provenance.
- NP396008.RAnoSWFJSSQP7XoK25I_wb108ZCXtWU9BiG7Huxr2yB_U130_assertion evidence source_evidence_literature NP396008.RAnoSWFJSSQP7XoK25I_wb108ZCXtWU9BiG7Huxr2yB_U130_provenance.
- NP396008.RAnoSWFJSSQP7XoK25I_wb108ZCXtWU9BiG7Huxr2yB_U130_assertion description "[A novel form of short QT syndrome (SQT3) is caused by a mutation in the KCNJ2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP396008.RAnoSWFJSSQP7XoK25I_wb108ZCXtWU9BiG7Huxr2yB_U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP396008.RAnoSWFJSSQP7XoK25I_wb108ZCXtWU9BiG7Huxr2yB_U130_provenance.