Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP683212.RAIdtRRtqFmdIYr77I2uWR4JVQ5J6DzL1_joLpQmhFPNE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP683212.RAIdtRRtqFmdIYr77I2uWR4JVQ5J6DzL1_joLpQmhFPNE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP683212.RAIdtRRtqFmdIYr77I2uWR4JVQ5J6DzL1_joLpQmhFPNE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP683212.RAIdtRRtqFmdIYr77I2uWR4JVQ5J6DzL1_joLpQmhFPNE130_provenance.
- NP683212.RAIdtRRtqFmdIYr77I2uWR4JVQ5J6DzL1_joLpQmhFPNE130_assertion description "[Mutations in the gene-encoding Na(v)1.5, SCN5A, have been associated with a variety of arrhythmic disorders, including long QT, Brugada, and sick sinus syndromes as well as progressive cardiac conduction defect and atrial standstill.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683212.RAIdtRRtqFmdIYr77I2uWR4JVQ5J6DzL1_joLpQmhFPNE130_provenance.
- NP683212.RAIdtRRtqFmdIYr77I2uWR4JVQ5J6DzL1_joLpQmhFPNE130_assertion evidence source_evidence_literature NP683212.RAIdtRRtqFmdIYr77I2uWR4JVQ5J6DzL1_joLpQmhFPNE130_provenance.
- NP683212.RAIdtRRtqFmdIYr77I2uWR4JVQ5J6DzL1_joLpQmhFPNE130_assertion SIO_000772 21937582 NP683212.RAIdtRRtqFmdIYr77I2uWR4JVQ5J6DzL1_joLpQmhFPNE130_provenance.
- NP683212.RAIdtRRtqFmdIYr77I2uWR4JVQ5J6DzL1_joLpQmhFPNE130_assertion wasDerivedFrom befree-20150227 NP683212.RAIdtRRtqFmdIYr77I2uWR4JVQ5J6DzL1_joLpQmhFPNE130_provenance.
- NP683212.RAIdtRRtqFmdIYr77I2uWR4JVQ5J6DzL1_joLpQmhFPNE130_assertion wasGeneratedBy ECO_0000203 NP683212.RAIdtRRtqFmdIYr77I2uWR4JVQ5J6DzL1_joLpQmhFPNE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP683212.RAIdtRRtqFmdIYr77I2uWR4JVQ5J6DzL1_joLpQmhFPNE130_provenance.