Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP109979.RAGyk3uR0YEIx338U0qBWNxuLtJs_kDjpWniFEiZOn0Sc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP109979.RAGyk3uR0YEIx338U0qBWNxuLtJs_kDjpWniFEiZOn0Sc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP109979.RAGyk3uR0YEIx338U0qBWNxuLtJs_kDjpWniFEiZOn0Sc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP109979.RAGyk3uR0YEIx338U0qBWNxuLtJs_kDjpWniFEiZOn0Sc130_provenance.
- NP109979.RAGyk3uR0YEIx338U0qBWNxuLtJs_kDjpWniFEiZOn0Sc130_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 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP109979.RAGyk3uR0YEIx338U0qBWNxuLtJs_kDjpWniFEiZOn0Sc130_provenance.
- NP109979.RAGyk3uR0YEIx338U0qBWNxuLtJs_kDjpWniFEiZOn0Sc130_assertion evidence source_evidence_literature NP109979.RAGyk3uR0YEIx338U0qBWNxuLtJs_kDjpWniFEiZOn0Sc130_provenance.
- NP109979.RAGyk3uR0YEIx338U0qBWNxuLtJs_kDjpWniFEiZOn0Sc130_assertion SIO_000772 20215590 NP109979.RAGyk3uR0YEIx338U0qBWNxuLtJs_kDjpWniFEiZOn0Sc130_provenance.
- NP109979.RAGyk3uR0YEIx338U0qBWNxuLtJs_kDjpWniFEiZOn0Sc130_assertion wasDerivedFrom gad-20150221 NP109979.RAGyk3uR0YEIx338U0qBWNxuLtJs_kDjpWniFEiZOn0Sc130_provenance.
- NP109979.RAGyk3uR0YEIx338U0qBWNxuLtJs_kDjpWniFEiZOn0Sc130_assertion wasGeneratedBy ECO_0000203 NP109979.RAGyk3uR0YEIx338U0qBWNxuLtJs_kDjpWniFEiZOn0Sc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP109979.RAGyk3uR0YEIx338U0qBWNxuLtJs_kDjpWniFEiZOn0Sc130_provenance.