Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP88121.RANCFUXPsJ1GbaX9VFacQ0P03qpQXKhTPLJByHo0hQe5c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP88121.RANCFUXPsJ1GbaX9VFacQ0P03qpQXKhTPLJByHo0hQe5c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP88121.RANCFUXPsJ1GbaX9VFacQ0P03qpQXKhTPLJByHo0hQe5c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP88121.RANCFUXPsJ1GbaX9VFacQ0P03qpQXKhTPLJByHo0hQe5c130_provenance.
- NP88121.RANCFUXPsJ1GbaX9VFacQ0P03qpQXKhTPLJByHo0hQe5c130_assertion description "[In this first study applying new TFC to patients suspected of ARVD/C, 64% of probable ARVD/C patients and 11% of family members were additionally diagnosed. ECG criteria and pathogenic mutations especially contributed to new diagnosis. Newly proposed TFC have a major impact in increasing diagnostic yield of ARVD/C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP88121.RANCFUXPsJ1GbaX9VFacQ0P03qpQXKhTPLJByHo0hQe5c130_provenance.
- NP88121.RANCFUXPsJ1GbaX9VFacQ0P03qpQXKhTPLJByHo0hQe5c130_assertion evidence source_evidence_literature NP88121.RANCFUXPsJ1GbaX9VFacQ0P03qpQXKhTPLJByHo0hQe5c130_provenance.
- NP88121.RANCFUXPsJ1GbaX9VFacQ0P03qpQXKhTPLJByHo0hQe5c130_assertion SIO_000772 20215590 NP88121.RANCFUXPsJ1GbaX9VFacQ0P03qpQXKhTPLJByHo0hQe5c130_provenance.
- NP88121.RANCFUXPsJ1GbaX9VFacQ0P03qpQXKhTPLJByHo0hQe5c130_assertion wasDerivedFrom gad-20130706 NP88121.RANCFUXPsJ1GbaX9VFacQ0P03qpQXKhTPLJByHo0hQe5c130_provenance.
- NP88121.RANCFUXPsJ1GbaX9VFacQ0P03qpQXKhTPLJByHo0hQe5c130_assertion wasGeneratedBy ECO_0000203 NP88121.RANCFUXPsJ1GbaX9VFacQ0P03qpQXKhTPLJByHo0hQe5c130_provenance.
- gad-20130706 importedOn "2013-07-06" NP88121.RANCFUXPsJ1GbaX9VFacQ0P03qpQXKhTPLJByHo0hQe5c130_provenance.