Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP35.RAaX_U_Va0-nQOnWe9eDF7PLScV21RlEqHSiIBz_lbp84130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP35.RAaX_U_Va0-nQOnWe9eDF7PLScV21RlEqHSiIBz_lbp84130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP35.RAaX_U_Va0-nQOnWe9eDF7PLScV21RlEqHSiIBz_lbp84130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP35.RAaX_U_Va0-nQOnWe9eDF7PLScV21RlEqHSiIBz_lbp84130_provenance.
- NP35.RAaX_U_Va0-nQOnWe9eDF7PLScV21RlEqHSiIBz_lbp84130_assertion description "[Abnormal electrophysiological findings in CNS pathway examinations should raise the suspicion of CMTX and a search for gene mutations towards Cx32 should be considered.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP35.RAaX_U_Va0-nQOnWe9eDF7PLScV21RlEqHSiIBz_lbp84130_provenance.
- NP35.RAaX_U_Va0-nQOnWe9eDF7PLScV21RlEqHSiIBz_lbp84130_assertion evidence source_evidence_curated NP35.RAaX_U_Va0-nQOnWe9eDF7PLScV21RlEqHSiIBz_lbp84130_provenance.
- NP35.RAaX_U_Va0-nQOnWe9eDF7PLScV21RlEqHSiIBz_lbp84130_assertion SIO_000772 10071100 NP35.RAaX_U_Va0-nQOnWe9eDF7PLScV21RlEqHSiIBz_lbp84130_provenance.
- NP35.RAaX_U_Va0-nQOnWe9eDF7PLScV21RlEqHSiIBz_lbp84130_assertion wasDerivedFrom uniprot-2016 NP35.RAaX_U_Va0-nQOnWe9eDF7PLScV21RlEqHSiIBz_lbp84130_provenance.
- NP35.RAaX_U_Va0-nQOnWe9eDF7PLScV21RlEqHSiIBz_lbp84130_assertion wasGeneratedBy ECO_0000218 NP35.RAaX_U_Va0-nQOnWe9eDF7PLScV21RlEqHSiIBz_lbp84130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP35.RAaX_U_Va0-nQOnWe9eDF7PLScV21RlEqHSiIBz_lbp84130_provenance.