Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP499093.RAyZDdvGcGcQ4HUxyLxAK2wot9hV5HJm3WmE5Z3SC9rE8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP499093.RAyZDdvGcGcQ4HUxyLxAK2wot9hV5HJm3WmE5Z3SC9rE8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP499093.RAyZDdvGcGcQ4HUxyLxAK2wot9hV5HJm3WmE5Z3SC9rE8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP499093.RAyZDdvGcGcQ4HUxyLxAK2wot9hV5HJm3WmE5Z3SC9rE8130_provenance.
- NP499093.RAyZDdvGcGcQ4HUxyLxAK2wot9hV5HJm3WmE5Z3SC9rE8130_assertion wasGeneratedBy ECO_0000203 NP499093.RAyZDdvGcGcQ4HUxyLxAK2wot9hV5HJm3WmE5Z3SC9rE8130_provenance.
- NP499093.RAyZDdvGcGcQ4HUxyLxAK2wot9hV5HJm3WmE5Z3SC9rE8130_assertion wasDerivedFrom befree-20140225 NP499093.RAyZDdvGcGcQ4HUxyLxAK2wot9hV5HJm3WmE5Z3SC9rE8130_provenance.
- NP499093.RAyZDdvGcGcQ4HUxyLxAK2wot9hV5HJm3WmE5Z3SC9rE8130_assertion SIO_000772 9243090 NP499093.RAyZDdvGcGcQ4HUxyLxAK2wot9hV5HJm3WmE5Z3SC9rE8130_provenance.
- NP499093.RAyZDdvGcGcQ4HUxyLxAK2wot9hV5HJm3WmE5Z3SC9rE8130_assertion evidence source_evidence_literature NP499093.RAyZDdvGcGcQ4HUxyLxAK2wot9hV5HJm3WmE5Z3SC9rE8130_provenance.
- NP499093.RAyZDdvGcGcQ4HUxyLxAK2wot9hV5HJm3WmE5Z3SC9rE8130_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." NP499093.RAyZDdvGcGcQ4HUxyLxAK2wot9hV5HJm3WmE5Z3SC9rE8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP499093.RAyZDdvGcGcQ4HUxyLxAK2wot9hV5HJm3WmE5Z3SC9rE8130_provenance.