Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP311446.RAqaD4vwrQ_68kw6qGWGNG0_AFu9LYn1-RDtrG5RB6gOU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP311446.RAqaD4vwrQ_68kw6qGWGNG0_AFu9LYn1-RDtrG5RB6gOU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP311446.RAqaD4vwrQ_68kw6qGWGNG0_AFu9LYn1-RDtrG5RB6gOU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP311446.RAqaD4vwrQ_68kw6qGWGNG0_AFu9LYn1-RDtrG5RB6gOU130_provenance.
- NP311446.RAqaD4vwrQ_68kw6qGWGNG0_AFu9LYn1-RDtrG5RB6gOU130_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." NP311446.RAqaD4vwrQ_68kw6qGWGNG0_AFu9LYn1-RDtrG5RB6gOU130_provenance.
- NP311446.RAqaD4vwrQ_68kw6qGWGNG0_AFu9LYn1-RDtrG5RB6gOU130_assertion evidence source_evidence_literature NP311446.RAqaD4vwrQ_68kw6qGWGNG0_AFu9LYn1-RDtrG5RB6gOU130_provenance.
- NP311446.RAqaD4vwrQ_68kw6qGWGNG0_AFu9LYn1-RDtrG5RB6gOU130_assertion SIO_000772 11257260 NP311446.RAqaD4vwrQ_68kw6qGWGNG0_AFu9LYn1-RDtrG5RB6gOU130_provenance.
- NP311446.RAqaD4vwrQ_68kw6qGWGNG0_AFu9LYn1-RDtrG5RB6gOU130_assertion wasDerivedFrom befree-2016 NP311446.RAqaD4vwrQ_68kw6qGWGNG0_AFu9LYn1-RDtrG5RB6gOU130_provenance.
- NP311446.RAqaD4vwrQ_68kw6qGWGNG0_AFu9LYn1-RDtrG5RB6gOU130_assertion wasGeneratedBy ECO_0000203 NP311446.RAqaD4vwrQ_68kw6qGWGNG0_AFu9LYn1-RDtrG5RB6gOU130_provenance.
- befree-2016 importedOn "2016-02-19" NP311446.RAqaD4vwrQ_68kw6qGWGNG0_AFu9LYn1-RDtrG5RB6gOU130_provenance.