Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP174099.RAtOi14ePeH4chWKFZrhJuYwp00A6JQGWaciMRdMiEloU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP174099.RAtOi14ePeH4chWKFZrhJuYwp00A6JQGWaciMRdMiEloU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP174099.RAtOi14ePeH4chWKFZrhJuYwp00A6JQGWaciMRdMiEloU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP174099.RAtOi14ePeH4chWKFZrhJuYwp00A6JQGWaciMRdMiEloU130_provenance.
- NP174099.RAtOi14ePeH4chWKFZrhJuYwp00A6JQGWaciMRdMiEloU130_assertion description "[Heterozygosity for the amyloidogenic TTR V122I mutation is relatively common in community-dwelling African Americans. Before the age of 65 years, the allele has no discernible impact on cardiac function or mortality. After the age of 70 years, carriers sh]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP174099.RAtOi14ePeH4chWKFZrhJuYwp00A6JQGWaciMRdMiEloU130_provenance.
- NP174099.RAtOi14ePeH4chWKFZrhJuYwp00A6JQGWaciMRdMiEloU130_assertion evidence source_evidence_literature NP174099.RAtOi14ePeH4chWKFZrhJuYwp00A6JQGWaciMRdMiEloU130_provenance.
- NP174099.RAtOi14ePeH4chWKFZrhJuYwp00A6JQGWaciMRdMiEloU130_assertion SIO_000772 20435197 NP174099.RAtOi14ePeH4chWKFZrhJuYwp00A6JQGWaciMRdMiEloU130_provenance.
- NP174099.RAtOi14ePeH4chWKFZrhJuYwp00A6JQGWaciMRdMiEloU130_assertion wasDerivedFrom gad-20150221 NP174099.RAtOi14ePeH4chWKFZrhJuYwp00A6JQGWaciMRdMiEloU130_provenance.
- NP174099.RAtOi14ePeH4chWKFZrhJuYwp00A6JQGWaciMRdMiEloU130_assertion wasGeneratedBy ECO_0000203 NP174099.RAtOi14ePeH4chWKFZrhJuYwp00A6JQGWaciMRdMiEloU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP174099.RAtOi14ePeH4chWKFZrhJuYwp00A6JQGWaciMRdMiEloU130_provenance.