Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP683038.RA0QgP7VD2S05Lpg9RVRxTs8swRLtRIHiLNGnyvqjVZAI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP683038.RA0QgP7VD2S05Lpg9RVRxTs8swRLtRIHiLNGnyvqjVZAI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP683038.RA0QgP7VD2S05Lpg9RVRxTs8swRLtRIHiLNGnyvqjVZAI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP683038.RA0QgP7VD2S05Lpg9RVRxTs8swRLtRIHiLNGnyvqjVZAI130_provenance.
- NP683038.RA0QgP7VD2S05Lpg9RVRxTs8swRLtRIHiLNGnyvqjVZAI130_assertion description "[Besides identifying 8 SCN5A mutations in the present cohort, a KCNE3 T4A mutation was found in a 55-year-old male patient who had experienced several episodes of syncope.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683038.RA0QgP7VD2S05Lpg9RVRxTs8swRLtRIHiLNGnyvqjVZAI130_provenance.
- NP683038.RA0QgP7VD2S05Lpg9RVRxTs8swRLtRIHiLNGnyvqjVZAI130_assertion evidence source_evidence_literature NP683038.RA0QgP7VD2S05Lpg9RVRxTs8swRLtRIHiLNGnyvqjVZAI130_provenance.
- NP683038.RA0QgP7VD2S05Lpg9RVRxTs8swRLtRIHiLNGnyvqjVZAI130_assertion SIO_000772 22987075 NP683038.RA0QgP7VD2S05Lpg9RVRxTs8swRLtRIHiLNGnyvqjVZAI130_provenance.
- NP683038.RA0QgP7VD2S05Lpg9RVRxTs8swRLtRIHiLNGnyvqjVZAI130_assertion wasDerivedFrom befree-20150227 NP683038.RA0QgP7VD2S05Lpg9RVRxTs8swRLtRIHiLNGnyvqjVZAI130_provenance.
- NP683038.RA0QgP7VD2S05Lpg9RVRxTs8swRLtRIHiLNGnyvqjVZAI130_assertion wasGeneratedBy ECO_0000203 NP683038.RA0QgP7VD2S05Lpg9RVRxTs8swRLtRIHiLNGnyvqjVZAI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP683038.RA0QgP7VD2S05Lpg9RVRxTs8swRLtRIHiLNGnyvqjVZAI130_provenance.