Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP134650.RACBzmS6OkKvfIb5LRRUjd7oPzGMkRBmfk6A5zzaKcunU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP134650.RACBzmS6OkKvfIb5LRRUjd7oPzGMkRBmfk6A5zzaKcunU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP134650.RACBzmS6OkKvfIb5LRRUjd7oPzGMkRBmfk6A5zzaKcunU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP134650.RACBzmS6OkKvfIb5LRRUjd7oPzGMkRBmfk6A5zzaKcunU130_provenance.
- NP134650.RACBzmS6OkKvfIb5LRRUjd7oPzGMkRBmfk6A5zzaKcunU130_assertion description "[These findings indicate that mutations in the ARX gene are very rare in autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP134650.RACBzmS6OkKvfIb5LRRUjd7oPzGMkRBmfk6A5zzaKcunU130_provenance.
- NP134650.RACBzmS6OkKvfIb5LRRUjd7oPzGMkRBmfk6A5zzaKcunU130_assertion evidence source_evidence_literature NP134650.RACBzmS6OkKvfIb5LRRUjd7oPzGMkRBmfk6A5zzaKcunU130_provenance.
- NP134650.RACBzmS6OkKvfIb5LRRUjd7oPzGMkRBmfk6A5zzaKcunU130_assertion SIO_000772 17044103 NP134650.RACBzmS6OkKvfIb5LRRUjd7oPzGMkRBmfk6A5zzaKcunU130_provenance.
- NP134650.RACBzmS6OkKvfIb5LRRUjd7oPzGMkRBmfk6A5zzaKcunU130_assertion wasDerivedFrom lhgdn-20090331 NP134650.RACBzmS6OkKvfIb5LRRUjd7oPzGMkRBmfk6A5zzaKcunU130_provenance.
- NP134650.RACBzmS6OkKvfIb5LRRUjd7oPzGMkRBmfk6A5zzaKcunU130_assertion wasGeneratedBy ECO_0000203 NP134650.RACBzmS6OkKvfIb5LRRUjd7oPzGMkRBmfk6A5zzaKcunU130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP134650.RACBzmS6OkKvfIb5LRRUjd7oPzGMkRBmfk6A5zzaKcunU130_provenance.