Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP654751.RAC3kAnpQA0YmLlsugvEqr0-28GwHQtNcafkkIYZxH0YI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP654751.RAC3kAnpQA0YmLlsugvEqr0-28GwHQtNcafkkIYZxH0YI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP654751.RAC3kAnpQA0YmLlsugvEqr0-28GwHQtNcafkkIYZxH0YI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP654751.RAC3kAnpQA0YmLlsugvEqr0-28GwHQtNcafkkIYZxH0YI130_provenance.
- NP654751.RAC3kAnpQA0YmLlsugvEqr0-28GwHQtNcafkkIYZxH0YI130_assertion description "[Recently, the coincidence of mutations in ACTA2 (vascular smooth muscle cell specific isoform of ?-actin) in families with thoracic aortic aneurysms and dissections (TAAD) and Moyamoya disease (MMD) was reported in patients of Northern European descent and a positive family history for TAAD and MMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP654751.RAC3kAnpQA0YmLlsugvEqr0-28GwHQtNcafkkIYZxH0YI130_provenance.
- NP654751.RAC3kAnpQA0YmLlsugvEqr0-28GwHQtNcafkkIYZxH0YI130_assertion evidence source_evidence_literature NP654751.RAC3kAnpQA0YmLlsugvEqr0-28GwHQtNcafkkIYZxH0YI130_provenance.
- NP654751.RAC3kAnpQA0YmLlsugvEqr0-28GwHQtNcafkkIYZxH0YI130_assertion SIO_000772 20970362 NP654751.RAC3kAnpQA0YmLlsugvEqr0-28GwHQtNcafkkIYZxH0YI130_provenance.
- NP654751.RAC3kAnpQA0YmLlsugvEqr0-28GwHQtNcafkkIYZxH0YI130_assertion wasDerivedFrom befree-20140225 NP654751.RAC3kAnpQA0YmLlsugvEqr0-28GwHQtNcafkkIYZxH0YI130_provenance.
- NP654751.RAC3kAnpQA0YmLlsugvEqr0-28GwHQtNcafkkIYZxH0YI130_assertion wasGeneratedBy ECO_0000203 NP654751.RAC3kAnpQA0YmLlsugvEqr0-28GwHQtNcafkkIYZxH0YI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP654751.RAC3kAnpQA0YmLlsugvEqr0-28GwHQtNcafkkIYZxH0YI130_provenance.