Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP668453.RAIH6aIc7Y1bCGnaWevSG12pDjXVFLguZSvRwxWMoyiNU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP668453.RAIH6aIc7Y1bCGnaWevSG12pDjXVFLguZSvRwxWMoyiNU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668453.RAIH6aIc7Y1bCGnaWevSG12pDjXVFLguZSvRwxWMoyiNU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668453.RAIH6aIc7Y1bCGnaWevSG12pDjXVFLguZSvRwxWMoyiNU130_provenance.
- NP668453.RAIH6aIc7Y1bCGnaWevSG12pDjXVFLguZSvRwxWMoyiNU130_assertion description "[CHD7 mutation spectrum in 28 Swedish patients diagnosed with CHARGE syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668453.RAIH6aIc7Y1bCGnaWevSG12pDjXVFLguZSvRwxWMoyiNU130_provenance.
- NP668453.RAIH6aIc7Y1bCGnaWevSG12pDjXVFLguZSvRwxWMoyiNU130_assertion evidence source_evidence_literature NP668453.RAIH6aIc7Y1bCGnaWevSG12pDjXVFLguZSvRwxWMoyiNU130_provenance.
- NP668453.RAIH6aIc7Y1bCGnaWevSG12pDjXVFLguZSvRwxWMoyiNU130_assertion SIO_000772 18445044 NP668453.RAIH6aIc7Y1bCGnaWevSG12pDjXVFLguZSvRwxWMoyiNU130_provenance.
- NP668453.RAIH6aIc7Y1bCGnaWevSG12pDjXVFLguZSvRwxWMoyiNU130_assertion wasDerivedFrom befree-2016 NP668453.RAIH6aIc7Y1bCGnaWevSG12pDjXVFLguZSvRwxWMoyiNU130_provenance.
- NP668453.RAIH6aIc7Y1bCGnaWevSG12pDjXVFLguZSvRwxWMoyiNU130_assertion wasGeneratedBy ECO_0000203 NP668453.RAIH6aIc7Y1bCGnaWevSG12pDjXVFLguZSvRwxWMoyiNU130_provenance.
- befree-2016 importedOn "2016-02-19" NP668453.RAIH6aIc7Y1bCGnaWevSG12pDjXVFLguZSvRwxWMoyiNU130_provenance.