Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP521032.RAqSpqC3_ccLN1ZEhQxBtO-NXgTP3l6D-qbgulbclgq8s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP521032.RAqSpqC3_ccLN1ZEhQxBtO-NXgTP3l6D-qbgulbclgq8s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP521032.RAqSpqC3_ccLN1ZEhQxBtO-NXgTP3l6D-qbgulbclgq8s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP521032.RAqSpqC3_ccLN1ZEhQxBtO-NXgTP3l6D-qbgulbclgq8s130_provenance.
- NP521032.RAqSpqC3_ccLN1ZEhQxBtO-NXgTP3l6D-qbgulbclgq8s130_assertion description "[We screened members of the Framingham Heart Study (FHS) for variation in three genes-SLC12A3 (NCCT), SLC12A1 (NKCC2) and KCNJ1 (ROMK)-causing rare recessive diseases featuring large reductions in blood pressure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP521032.RAqSpqC3_ccLN1ZEhQxBtO-NXgTP3l6D-qbgulbclgq8s130_provenance.
- NP521032.RAqSpqC3_ccLN1ZEhQxBtO-NXgTP3l6D-qbgulbclgq8s130_assertion evidence source_evidence_literature NP521032.RAqSpqC3_ccLN1ZEhQxBtO-NXgTP3l6D-qbgulbclgq8s130_provenance.
- NP521032.RAqSpqC3_ccLN1ZEhQxBtO-NXgTP3l6D-qbgulbclgq8s130_assertion SIO_000772 18391953 NP521032.RAqSpqC3_ccLN1ZEhQxBtO-NXgTP3l6D-qbgulbclgq8s130_provenance.
- NP521032.RAqSpqC3_ccLN1ZEhQxBtO-NXgTP3l6D-qbgulbclgq8s130_assertion wasDerivedFrom befree-20140225 NP521032.RAqSpqC3_ccLN1ZEhQxBtO-NXgTP3l6D-qbgulbclgq8s130_provenance.
- NP521032.RAqSpqC3_ccLN1ZEhQxBtO-NXgTP3l6D-qbgulbclgq8s130_assertion wasGeneratedBy ECO_0000203 NP521032.RAqSpqC3_ccLN1ZEhQxBtO-NXgTP3l6D-qbgulbclgq8s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP521032.RAqSpqC3_ccLN1ZEhQxBtO-NXgTP3l6D-qbgulbclgq8s130_provenance.