Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP581821.RA3PJbTS7CpDE3Q-pLyj4Iu2hrpNLH3pWTQP3OYfocdM0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP581821.RA3PJbTS7CpDE3Q-pLyj4Iu2hrpNLH3pWTQP3OYfocdM0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP581821.RA3PJbTS7CpDE3Q-pLyj4Iu2hrpNLH3pWTQP3OYfocdM0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP581821.RA3PJbTS7CpDE3Q-pLyj4Iu2hrpNLH3pWTQP3OYfocdM0130_provenance.
- befree-2016 importedOn "2016-02-19" NP581821.RA3PJbTS7CpDE3Q-pLyj4Iu2hrpNLH3pWTQP3OYfocdM0130_provenance.
- NP581821.RA3PJbTS7CpDE3Q-pLyj4Iu2hrpNLH3pWTQP3OYfocdM0130_assertion wasGeneratedBy ECO_0000203 NP581821.RA3PJbTS7CpDE3Q-pLyj4Iu2hrpNLH3pWTQP3OYfocdM0130_provenance.
- NP581821.RA3PJbTS7CpDE3Q-pLyj4Iu2hrpNLH3pWTQP3OYfocdM0130_assertion wasDerivedFrom befree-2016 NP581821.RA3PJbTS7CpDE3Q-pLyj4Iu2hrpNLH3pWTQP3OYfocdM0130_provenance.
- NP581821.RA3PJbTS7CpDE3Q-pLyj4Iu2hrpNLH3pWTQP3OYfocdM0130_assertion SIO_000772 17136396 NP581821.RA3PJbTS7CpDE3Q-pLyj4Iu2hrpNLH3pWTQP3OYfocdM0130_provenance.
- NP581821.RA3PJbTS7CpDE3Q-pLyj4Iu2hrpNLH3pWTQP3OYfocdM0130_assertion evidence source_evidence_literature NP581821.RA3PJbTS7CpDE3Q-pLyj4Iu2hrpNLH3pWTQP3OYfocdM0130_provenance.
- NP581821.RA3PJbTS7CpDE3Q-pLyj4Iu2hrpNLH3pWTQP3OYfocdM0130_assertion description "[Functional analysis of a novel potassium channel (KCNA1) mutation in hereditary myokymia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP581821.RA3PJbTS7CpDE3Q-pLyj4Iu2hrpNLH3pWTQP3OYfocdM0130_provenance.