Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP700077.RAmTOj-58QoVFd3o3kw-lUOh8lTsUWG80GDER7lcs4DDA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP700077.RAmTOj-58QoVFd3o3kw-lUOh8lTsUWG80GDER7lcs4DDA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP700077.RAmTOj-58QoVFd3o3kw-lUOh8lTsUWG80GDER7lcs4DDA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP700077.RAmTOj-58QoVFd3o3kw-lUOh8lTsUWG80GDER7lcs4DDA130_provenance.
- NP700077.RAmTOj-58QoVFd3o3kw-lUOh8lTsUWG80GDER7lcs4DDA130_assertion wasGeneratedBy ECO_0000203 NP700077.RAmTOj-58QoVFd3o3kw-lUOh8lTsUWG80GDER7lcs4DDA130_provenance.
- NP700077.RAmTOj-58QoVFd3o3kw-lUOh8lTsUWG80GDER7lcs4DDA130_assertion wasDerivedFrom befree-20140225 NP700077.RAmTOj-58QoVFd3o3kw-lUOh8lTsUWG80GDER7lcs4DDA130_provenance.
- NP700077.RAmTOj-58QoVFd3o3kw-lUOh8lTsUWG80GDER7lcs4DDA130_assertion SIO_000772 18721526 NP700077.RAmTOj-58QoVFd3o3kw-lUOh8lTsUWG80GDER7lcs4DDA130_provenance.
- NP700077.RAmTOj-58QoVFd3o3kw-lUOh8lTsUWG80GDER7lcs4DDA130_assertion evidence source_evidence_literature NP700077.RAmTOj-58QoVFd3o3kw-lUOh8lTsUWG80GDER7lcs4DDA130_provenance.
- NP700077.RAmTOj-58QoVFd3o3kw-lUOh8lTsUWG80GDER7lcs4DDA130_assertion description "[Because bicuspid aortic valve (BAV) is a congenital heart defect in patients with Loeys-Dietz syndrome, this study was conducted to investigate whether variants in TGFBR1 or TGFBR2 are responsible for sporadic BAV.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP700077.RAmTOj-58QoVFd3o3kw-lUOh8lTsUWG80GDER7lcs4DDA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP700077.RAmTOj-58QoVFd3o3kw-lUOh8lTsUWG80GDER7lcs4DDA130_provenance.