Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP149461.RAvpCdzNrcU4HXkMqez655C6oCMa1aG1pneMdMYStqf8Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP149461.RAvpCdzNrcU4HXkMqez655C6oCMa1aG1pneMdMYStqf8Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP149461.RAvpCdzNrcU4HXkMqez655C6oCMa1aG1pneMdMYStqf8Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP149461.RAvpCdzNrcU4HXkMqez655C6oCMa1aG1pneMdMYStqf8Q130_provenance.
- NP149461.RAvpCdzNrcU4HXkMqez655C6oCMa1aG1pneMdMYStqf8Q130_assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common frequency of pulmonary arteriovenous malformations in patients with ENG mutations than in patients with ACVRL1 mutations in our collective.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149461.RAvpCdzNrcU4HXkMqez655C6oCMa1aG1pneMdMYStqf8Q130_provenance.
- NP149461.RAvpCdzNrcU4HXkMqez655C6oCMa1aG1pneMdMYStqf8Q130_assertion evidence source_evidence_literature NP149461.RAvpCdzNrcU4HXkMqez655C6oCMa1aG1pneMdMYStqf8Q130_provenance.
- NP149461.RAvpCdzNrcU4HXkMqez655C6oCMa1aG1pneMdMYStqf8Q130_assertion SIO_000772 16542389 NP149461.RAvpCdzNrcU4HXkMqez655C6oCMa1aG1pneMdMYStqf8Q130_provenance.
- NP149461.RAvpCdzNrcU4HXkMqez655C6oCMa1aG1pneMdMYStqf8Q130_assertion wasDerivedFrom lhgdn-20090331 NP149461.RAvpCdzNrcU4HXkMqez655C6oCMa1aG1pneMdMYStqf8Q130_provenance.
- NP149461.RAvpCdzNrcU4HXkMqez655C6oCMa1aG1pneMdMYStqf8Q130_assertion wasGeneratedBy ECO_0000203 NP149461.RAvpCdzNrcU4HXkMqez655C6oCMa1aG1pneMdMYStqf8Q130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP149461.RAvpCdzNrcU4HXkMqez655C6oCMa1aG1pneMdMYStqf8Q130_provenance.