Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP977341.RAkI5XYJznYK8ZhNKemkTw0rY_9Wq52bx9WzxMwDyog-o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP977341.RAkI5XYJznYK8ZhNKemkTw0rY_9Wq52bx9WzxMwDyog-o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977341.RAkI5XYJznYK8ZhNKemkTw0rY_9Wq52bx9WzxMwDyog-o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977341.RAkI5XYJznYK8ZhNKemkTw0rY_9Wq52bx9WzxMwDyog-o130_provenance.
- NP977341.RAkI5XYJznYK8ZhNKemkTw0rY_9Wq52bx9WzxMwDyog-o130_assertion description "[The affected boy, who possesses mutant HSD10 (p.V65A), has a neurological syndrome with metabolic derangements, choreoathetosis, refractory epilepsy and learning disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977341.RAkI5XYJznYK8ZhNKemkTw0rY_9Wq52bx9WzxMwDyog-o130_provenance.
- NP977341.RAkI5XYJznYK8ZhNKemkTw0rY_9Wq52bx9WzxMwDyog-o130_assertion evidence source_evidence_literature NP977341.RAkI5XYJznYK8ZhNKemkTw0rY_9Wq52bx9WzxMwDyog-o130_provenance.
- NP977341.RAkI5XYJznYK8ZhNKemkTw0rY_9Wq52bx9WzxMwDyog-o130_assertion SIO_000772 22132097 NP977341.RAkI5XYJznYK8ZhNKemkTw0rY_9Wq52bx9WzxMwDyog-o130_provenance.
- NP977341.RAkI5XYJznYK8ZhNKemkTw0rY_9Wq52bx9WzxMwDyog-o130_assertion wasDerivedFrom befree-20150227 NP977341.RAkI5XYJznYK8ZhNKemkTw0rY_9Wq52bx9WzxMwDyog-o130_provenance.
- NP977341.RAkI5XYJznYK8ZhNKemkTw0rY_9Wq52bx9WzxMwDyog-o130_assertion wasGeneratedBy ECO_0000203 NP977341.RAkI5XYJznYK8ZhNKemkTw0rY_9Wq52bx9WzxMwDyog-o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP977341.RAkI5XYJznYK8ZhNKemkTw0rY_9Wq52bx9WzxMwDyog-o130_provenance.