Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP393556.RA3klmXfPIph49E43mYq962ue8tK4AZusYhtVLs1m_ILs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP393556.RA3klmXfPIph49E43mYq962ue8tK4AZusYhtVLs1m_ILs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP393556.RA3klmXfPIph49E43mYq962ue8tK4AZusYhtVLs1m_ILs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP393556.RA3klmXfPIph49E43mYq962ue8tK4AZusYhtVLs1m_ILs130_provenance.
- befree-2016 importedOn "2016-02-19" NP393556.RA3klmXfPIph49E43mYq962ue8tK4AZusYhtVLs1m_ILs130_provenance.
- NP393556.RA3klmXfPIph49E43mYq962ue8tK4AZusYhtVLs1m_ILs130_assertion wasGeneratedBy ECO_0000203 NP393556.RA3klmXfPIph49E43mYq962ue8tK4AZusYhtVLs1m_ILs130_provenance.
- NP393556.RA3klmXfPIph49E43mYq962ue8tK4AZusYhtVLs1m_ILs130_assertion wasDerivedFrom befree-2016 NP393556.RA3klmXfPIph49E43mYq962ue8tK4AZusYhtVLs1m_ILs130_provenance.
- NP393556.RA3klmXfPIph49E43mYq962ue8tK4AZusYhtVLs1m_ILs130_assertion SIO_000772 12736279 NP393556.RA3klmXfPIph49E43mYq962ue8tK4AZusYhtVLs1m_ILs130_provenance.
- NP393556.RA3klmXfPIph49E43mYq962ue8tK4AZusYhtVLs1m_ILs130_assertion evidence source_evidence_literature NP393556.RA3klmXfPIph49E43mYq962ue8tK4AZusYhtVLs1m_ILs130_provenance.
- NP393556.RA3klmXfPIph49E43mYq962ue8tK4AZusYhtVLs1m_ILs130_assertion description "[We evaluated 647 patients (386 with a mutation at the LQT1 locus, 206 with a mutation at the LQT2 locus, and 55 with a mutation at the LQT3 locus) from 193 consecutively genotyped families with the long-QT syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP393556.RA3klmXfPIph49E43mYq962ue8tK4AZusYhtVLs1m_ILs130_provenance.