Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP787830.RA0LihUnW_TsLV5v4-O13CgchzQMNfFI7FRl0pZt92NC8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP787830.RA0LihUnW_TsLV5v4-O13CgchzQMNfFI7FRl0pZt92NC8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP787830.RA0LihUnW_TsLV5v4-O13CgchzQMNfFI7FRl0pZt92NC8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP787830.RA0LihUnW_TsLV5v4-O13CgchzQMNfFI7FRl0pZt92NC8130_provenance.
- NP787830.RA0LihUnW_TsLV5v4-O13CgchzQMNfFI7FRl0pZt92NC8130_assertion description "[The following were performed: genotyping of banked DNA for TTR V122I allele status and review of cardiovascular and demographic parameters in CHS and ARIC databases, with statistical comparisons of the frequency of congestive heart failure, survival, and occurrence of features of cardiac amyloidosis in carriers of the amyloidogenic allele and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787830.RA0LihUnW_TsLV5v4-O13CgchzQMNfFI7FRl0pZt92NC8130_provenance.
- NP787830.RA0LihUnW_TsLV5v4-O13CgchzQMNfFI7FRl0pZt92NC8130_assertion evidence source_evidence_literature NP787830.RA0LihUnW_TsLV5v4-O13CgchzQMNfFI7FRl0pZt92NC8130_provenance.
- NP787830.RA0LihUnW_TsLV5v4-O13CgchzQMNfFI7FRl0pZt92NC8130_assertion SIO_000772 20435197 NP787830.RA0LihUnW_TsLV5v4-O13CgchzQMNfFI7FRl0pZt92NC8130_provenance.
- NP787830.RA0LihUnW_TsLV5v4-O13CgchzQMNfFI7FRl0pZt92NC8130_assertion wasDerivedFrom befree-20140225 NP787830.RA0LihUnW_TsLV5v4-O13CgchzQMNfFI7FRl0pZt92NC8130_provenance.
- NP787830.RA0LihUnW_TsLV5v4-O13CgchzQMNfFI7FRl0pZt92NC8130_assertion wasGeneratedBy ECO_0000203 NP787830.RA0LihUnW_TsLV5v4-O13CgchzQMNfFI7FRl0pZt92NC8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP787830.RA0LihUnW_TsLV5v4-O13CgchzQMNfFI7FRl0pZt92NC8130_provenance.