Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP603294.RAJ6W3sgCb7-pILDIH3kGvUNMESZbW95nXWGW0Ar0Yl1Y130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP603294.RAJ6W3sgCb7-pILDIH3kGvUNMESZbW95nXWGW0Ar0Yl1Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP603294.RAJ6W3sgCb7-pILDIH3kGvUNMESZbW95nXWGW0Ar0Yl1Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP603294.RAJ6W3sgCb7-pILDIH3kGvUNMESZbW95nXWGW0Ar0Yl1Y130_provenance.
- NP603294.RAJ6W3sgCb7-pILDIH3kGvUNMESZbW95nXWGW0Ar0Yl1Y130_assertion wasGeneratedBy ECO_0000203 NP603294.RAJ6W3sgCb7-pILDIH3kGvUNMESZbW95nXWGW0Ar0Yl1Y130_provenance.
- NP603294.RAJ6W3sgCb7-pILDIH3kGvUNMESZbW95nXWGW0Ar0Yl1Y130_assertion wasDerivedFrom befree-20140225 NP603294.RAJ6W3sgCb7-pILDIH3kGvUNMESZbW95nXWGW0Ar0Yl1Y130_provenance.
- NP603294.RAJ6W3sgCb7-pILDIH3kGvUNMESZbW95nXWGW0Ar0Yl1Y130_assertion SIO_000772 9243090 NP603294.RAJ6W3sgCb7-pILDIH3kGvUNMESZbW95nXWGW0Ar0Yl1Y130_provenance.
- NP603294.RAJ6W3sgCb7-pILDIH3kGvUNMESZbW95nXWGW0Ar0Yl1Y130_assertion evidence source_evidence_literature NP603294.RAJ6W3sgCb7-pILDIH3kGvUNMESZbW95nXWGW0Ar0Yl1Y130_provenance.
- NP603294.RAJ6W3sgCb7-pILDIH3kGvUNMESZbW95nXWGW0Ar0Yl1Y130_assertion description "[Deletions were rare among patients lacking typical DiGeorge syndrome (DGS) or velocardiofacial (VCF) dysmorphic features, and more common in tetralogy of Fallot with pulmonary atresia than tetralogy of Fallot alone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP603294.RAJ6W3sgCb7-pILDIH3kGvUNMESZbW95nXWGW0Ar0Yl1Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP603294.RAJ6W3sgCb7-pILDIH3kGvUNMESZbW95nXWGW0Ar0Yl1Y130_provenance.