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- source_evidence_literature type ECO_0000212 NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_provenance.
- NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_assertion wasGeneratedBy ECO_0000203 NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_provenance.
- NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_assertion wasDerivedFrom befree-20140225 NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_provenance.
- NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_assertion SIO_000772 10688323 NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_provenance.
- NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_assertion evidence source_evidence_literature NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_provenance.
- NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_assertion description "[Genetic studies have identified four forms of congenital long QT syndrome (LQTS) caused by mutations in ion channel genes located on chromosomes 3 (LQT3), 7 (LQT2), 11 (LQT1), and 21 (LQT5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP789268.RA7_DLbTQOawl4vjm5N3C_E8UwjMEE-NMzXGe-pjLoJDQ130_provenance.