Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP324878.RAA0WLOuhQfcw1XErKgg7_jp1VDlEF9m5Raukow-uLnSE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP324878.RAA0WLOuhQfcw1XErKgg7_jp1VDlEF9m5Raukow-uLnSE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP324878.RAA0WLOuhQfcw1XErKgg7_jp1VDlEF9m5Raukow-uLnSE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP324878.RAA0WLOuhQfcw1XErKgg7_jp1VDlEF9m5Raukow-uLnSE130_provenance.
- NP324878.RAA0WLOuhQfcw1XErKgg7_jp1VDlEF9m5Raukow-uLnSE130_assertion description "[Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324878.RAA0WLOuhQfcw1XErKgg7_jp1VDlEF9m5Raukow-uLnSE130_provenance.
- NP324878.RAA0WLOuhQfcw1XErKgg7_jp1VDlEF9m5Raukow-uLnSE130_assertion evidence source_evidence_literature NP324878.RAA0WLOuhQfcw1XErKgg7_jp1VDlEF9m5Raukow-uLnSE130_provenance.
- NP324878.RAA0WLOuhQfcw1XErKgg7_jp1VDlEF9m5Raukow-uLnSE130_assertion SIO_000772 11468227 NP324878.RAA0WLOuhQfcw1XErKgg7_jp1VDlEF9m5Raukow-uLnSE130_provenance.
- NP324878.RAA0WLOuhQfcw1XErKgg7_jp1VDlEF9m5Raukow-uLnSE130_assertion wasDerivedFrom befree-2016 NP324878.RAA0WLOuhQfcw1XErKgg7_jp1VDlEF9m5Raukow-uLnSE130_provenance.
- NP324878.RAA0WLOuhQfcw1XErKgg7_jp1VDlEF9m5Raukow-uLnSE130_assertion wasGeneratedBy ECO_0000203 NP324878.RAA0WLOuhQfcw1XErKgg7_jp1VDlEF9m5Raukow-uLnSE130_provenance.
- befree-2016 importedOn "2016-02-19" NP324878.RAA0WLOuhQfcw1XErKgg7_jp1VDlEF9m5Raukow-uLnSE130_provenance.