Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP498984.RAicTAW5suYi-VRIpNg5VFG8odFA3ixW42oC_L9QcigeI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP498984.RAicTAW5suYi-VRIpNg5VFG8odFA3ixW42oC_L9QcigeI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP498984.RAicTAW5suYi-VRIpNg5VFG8odFA3ixW42oC_L9QcigeI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP498984.RAicTAW5suYi-VRIpNg5VFG8odFA3ixW42oC_L9QcigeI130_provenance.
- NP498984.RAicTAW5suYi-VRIpNg5VFG8odFA3ixW42oC_L9QcigeI130_assertion description "[Dominant-negative I(Ks) suppression by KCNQ1-deltaF339 potassium channels linked to Romano-Ward syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP498984.RAicTAW5suYi-VRIpNg5VFG8odFA3ixW42oC_L9QcigeI130_provenance.
- NP498984.RAicTAW5suYi-VRIpNg5VFG8odFA3ixW42oC_L9QcigeI130_assertion evidence source_evidence_literature NP498984.RAicTAW5suYi-VRIpNg5VFG8odFA3ixW42oC_L9QcigeI130_provenance.
- NP498984.RAicTAW5suYi-VRIpNg5VFG8odFA3ixW42oC_L9QcigeI130_assertion SIO_000772 15950200 NP498984.RAicTAW5suYi-VRIpNg5VFG8odFA3ixW42oC_L9QcigeI130_provenance.
- NP498984.RAicTAW5suYi-VRIpNg5VFG8odFA3ixW42oC_L9QcigeI130_assertion wasDerivedFrom befree-2016 NP498984.RAicTAW5suYi-VRIpNg5VFG8odFA3ixW42oC_L9QcigeI130_provenance.
- NP498984.RAicTAW5suYi-VRIpNg5VFG8odFA3ixW42oC_L9QcigeI130_assertion wasGeneratedBy ECO_0000203 NP498984.RAicTAW5suYi-VRIpNg5VFG8odFA3ixW42oC_L9QcigeI130_provenance.
- befree-2016 importedOn "2016-02-19" NP498984.RAicTAW5suYi-VRIpNg5VFG8odFA3ixW42oC_L9QcigeI130_provenance.