Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP988068.RA6mccI1FDxbE5zfIfApnfMq2NqyWM9zAVdl1L7isz1xk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP988068.RA6mccI1FDxbE5zfIfApnfMq2NqyWM9zAVdl1L7isz1xk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP988068.RA6mccI1FDxbE5zfIfApnfMq2NqyWM9zAVdl1L7isz1xk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP988068.RA6mccI1FDxbE5zfIfApnfMq2NqyWM9zAVdl1L7isz1xk130_provenance.
- NP988068.RA6mccI1FDxbE5zfIfApnfMq2NqyWM9zAVdl1L7isz1xk130_assertion description "[Using polymerase chain reaction, denaturing high-performance liquid chromatography, and DNA sequencing, a comprehensive mutational analysis of the long QT syndrome susceptibility genes (KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2) and a targeted analysis of the catecholaminergic polymorphic ventricular tachycardia type 1-associated gene (RYR2) were conducted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP988068.RA6mccI1FDxbE5zfIfApnfMq2NqyWM9zAVdl1L7isz1xk130_provenance.
- NP988068.RA6mccI1FDxbE5zfIfApnfMq2NqyWM9zAVdl1L7isz1xk130_assertion evidence source_evidence_literature NP988068.RA6mccI1FDxbE5zfIfApnfMq2NqyWM9zAVdl1L7isz1xk130_provenance.
- NP988068.RA6mccI1FDxbE5zfIfApnfMq2NqyWM9zAVdl1L7isz1xk130_assertion SIO_000772 22677073 NP988068.RA6mccI1FDxbE5zfIfApnfMq2NqyWM9zAVdl1L7isz1xk130_provenance.
- NP988068.RA6mccI1FDxbE5zfIfApnfMq2NqyWM9zAVdl1L7isz1xk130_assertion wasDerivedFrom befree-2016 NP988068.RA6mccI1FDxbE5zfIfApnfMq2NqyWM9zAVdl1L7isz1xk130_provenance.
- NP988068.RA6mccI1FDxbE5zfIfApnfMq2NqyWM9zAVdl1L7isz1xk130_assertion wasGeneratedBy ECO_0000203 NP988068.RA6mccI1FDxbE5zfIfApnfMq2NqyWM9zAVdl1L7isz1xk130_provenance.
- befree-2016 importedOn "2016-02-19" NP988068.RA6mccI1FDxbE5zfIfApnfMq2NqyWM9zAVdl1L7isz1xk130_provenance.