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- source_evidence_literature type ECO_0000212 NP690024.RANivuFkmT9zA7Eis7A7v8xoLHl-bBJPYKbewaKCwrMK8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690024.RANivuFkmT9zA7Eis7A7v8xoLHl-bBJPYKbewaKCwrMK8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690024.RANivuFkmT9zA7Eis7A7v8xoLHl-bBJPYKbewaKCwrMK8130_provenance.
- NP690024.RANivuFkmT9zA7Eis7A7v8xoLHl-bBJPYKbewaKCwrMK8130_assertion description "[Mutations in the KCNQ1, HERG, SCN5A, minK and MiRP1 genes cause long QT syndrome (LQTS), of which there are two forms: the Romano Ward syndrome and the Jervell and Lange-Nielsen syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690024.RANivuFkmT9zA7Eis7A7v8xoLHl-bBJPYKbewaKCwrMK8130_provenance.
- NP690024.RANivuFkmT9zA7Eis7A7v8xoLHl-bBJPYKbewaKCwrMK8130_assertion evidence source_evidence_literature NP690024.RANivuFkmT9zA7Eis7A7v8xoLHl-bBJPYKbewaKCwrMK8130_provenance.
- NP690024.RANivuFkmT9zA7Eis7A7v8xoLHl-bBJPYKbewaKCwrMK8130_assertion SIO_000772 18752142 NP690024.RANivuFkmT9zA7Eis7A7v8xoLHl-bBJPYKbewaKCwrMK8130_provenance.
- NP690024.RANivuFkmT9zA7Eis7A7v8xoLHl-bBJPYKbewaKCwrMK8130_assertion wasDerivedFrom befree-2016 NP690024.RANivuFkmT9zA7Eis7A7v8xoLHl-bBJPYKbewaKCwrMK8130_provenance.
- NP690024.RANivuFkmT9zA7Eis7A7v8xoLHl-bBJPYKbewaKCwrMK8130_assertion wasGeneratedBy ECO_0000203 NP690024.RANivuFkmT9zA7Eis7A7v8xoLHl-bBJPYKbewaKCwrMK8130_provenance.
- befree-2016 importedOn "2016-02-19" NP690024.RANivuFkmT9zA7Eis7A7v8xoLHl-bBJPYKbewaKCwrMK8130_provenance.