Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP167096.RAFAVhLkBVtEYyMDUlr-SsbictjliUrcHTbdnC_iYQmXk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP167096.RAFAVhLkBVtEYyMDUlr-SsbictjliUrcHTbdnC_iYQmXk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP167096.RAFAVhLkBVtEYyMDUlr-SsbictjliUrcHTbdnC_iYQmXk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP167096.RAFAVhLkBVtEYyMDUlr-SsbictjliUrcHTbdnC_iYQmXk130_provenance.
- NP167096.RAFAVhLkBVtEYyMDUlr-SsbictjliUrcHTbdnC_iYQmXk130_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." NP167096.RAFAVhLkBVtEYyMDUlr-SsbictjliUrcHTbdnC_iYQmXk130_provenance.
- NP167096.RAFAVhLkBVtEYyMDUlr-SsbictjliUrcHTbdnC_iYQmXk130_assertion evidence source_evidence_literature NP167096.RAFAVhLkBVtEYyMDUlr-SsbictjliUrcHTbdnC_iYQmXk130_provenance.
- NP167096.RAFAVhLkBVtEYyMDUlr-SsbictjliUrcHTbdnC_iYQmXk130_assertion SIO_000772 20215590 NP167096.RAFAVhLkBVtEYyMDUlr-SsbictjliUrcHTbdnC_iYQmXk130_provenance.
- NP167096.RAFAVhLkBVtEYyMDUlr-SsbictjliUrcHTbdnC_iYQmXk130_assertion wasDerivedFrom gad-20150221 NP167096.RAFAVhLkBVtEYyMDUlr-SsbictjliUrcHTbdnC_iYQmXk130_provenance.
- NP167096.RAFAVhLkBVtEYyMDUlr-SsbictjliUrcHTbdnC_iYQmXk130_assertion wasGeneratedBy ECO_0000203 NP167096.RAFAVhLkBVtEYyMDUlr-SsbictjliUrcHTbdnC_iYQmXk130_provenance.
- gad-20150221 importedOn "2015-02-21" NP167096.RAFAVhLkBVtEYyMDUlr-SsbictjliUrcHTbdnC_iYQmXk130_provenance.