Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1334.RAnuYQr5Xs8JyMuV2awWnSUmQjPX9AO4WZsUCvU4FZuYA130_assertion> ?p ?o ?g. }
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- NP1334.RAnuYQr5Xs8JyMuV2awWnSUmQjPX9AO4WZsUCvU4FZuYA130_assertion type Assertion NP1334.RAnuYQr5Xs8JyMuV2awWnSUmQjPX9AO4WZsUCvU4FZuYA130_head.
- NP1334.RAnuYQr5Xs8JyMuV2awWnSUmQjPX9AO4WZsUCvU4FZuYA130_assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1334.RAnuYQr5Xs8JyMuV2awWnSUmQjPX9AO4WZsUCvU4FZuYA130_provenance.
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- NP1334.RAnuYQr5Xs8JyMuV2awWnSUmQjPX9AO4WZsUCvU4FZuYA130_assertion wasDerivedFrom uniprot-2016 NP1334.RAnuYQr5Xs8JyMuV2awWnSUmQjPX9AO4WZsUCvU4FZuYA130_provenance.
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