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- source_evidence_literature type ECO_0000212 NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_provenance.
- NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_assertion description "[Mutations in the hminK gene cause long QT syndrome and suppress IKs function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_provenance.
- NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_assertion evidence source_evidence_literature NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_provenance.
- NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_assertion SIO_000772 9354802 NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_provenance.
- NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_assertion wasDerivedFrom befree-20150227 NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_provenance.
- NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_assertion wasGeneratedBy ECO_0000203 NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP897310.RANQojI-DsbBKRDMS0hvYlxDp87-1QZwZy49iCDpAqclo130_provenance.