Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1125755.RAEXKgfJQ7AKesgp9ScDPr0BwsWEK51Nn8vMDGSRpbL5w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1125755.RAEXKgfJQ7AKesgp9ScDPr0BwsWEK51Nn8vMDGSRpbL5w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1125755.RAEXKgfJQ7AKesgp9ScDPr0BwsWEK51Nn8vMDGSRpbL5w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1125755.RAEXKgfJQ7AKesgp9ScDPr0BwsWEK51Nn8vMDGSRpbL5w130_provenance.
- NP1125755.RAEXKgfJQ7AKesgp9ScDPr0BwsWEK51Nn8vMDGSRpbL5w130_assertion description "[The recent HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited arrhythmia syndromes has updated the clinical diagnosis of congenital LQTS and BrS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1125755.RAEXKgfJQ7AKesgp9ScDPr0BwsWEK51Nn8vMDGSRpbL5w130_provenance.
- NP1125755.RAEXKgfJQ7AKesgp9ScDPr0BwsWEK51Nn8vMDGSRpbL5w130_assertion evidence source_evidence_literature NP1125755.RAEXKgfJQ7AKesgp9ScDPr0BwsWEK51Nn8vMDGSRpbL5w130_provenance.
- NP1125755.RAEXKgfJQ7AKesgp9ScDPr0BwsWEK51Nn8vMDGSRpbL5w130_assertion SIO_000772 24200848 NP1125755.RAEXKgfJQ7AKesgp9ScDPr0BwsWEK51Nn8vMDGSRpbL5w130_provenance.
- NP1125755.RAEXKgfJQ7AKesgp9ScDPr0BwsWEK51Nn8vMDGSRpbL5w130_assertion wasDerivedFrom befree-2016 NP1125755.RAEXKgfJQ7AKesgp9ScDPr0BwsWEK51Nn8vMDGSRpbL5w130_provenance.
- NP1125755.RAEXKgfJQ7AKesgp9ScDPr0BwsWEK51Nn8vMDGSRpbL5w130_assertion wasGeneratedBy ECO_0000203 NP1125755.RAEXKgfJQ7AKesgp9ScDPr0BwsWEK51Nn8vMDGSRpbL5w130_provenance.
- befree-2016 importedOn "2016-02-19" NP1125755.RAEXKgfJQ7AKesgp9ScDPr0BwsWEK51Nn8vMDGSRpbL5w130_provenance.