Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP190194.RAvD5efm3NeHMEB117TYyvPUMFKbXFy8YGxRHpLyEelkA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP190194.RAvD5efm3NeHMEB117TYyvPUMFKbXFy8YGxRHpLyEelkA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP190194.RAvD5efm3NeHMEB117TYyvPUMFKbXFy8YGxRHpLyEelkA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP190194.RAvD5efm3NeHMEB117TYyvPUMFKbXFy8YGxRHpLyEelkA130_provenance.
- NP190194.RAvD5efm3NeHMEB117TYyvPUMFKbXFy8YGxRHpLyEelkA130_assertion description "[Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP190194.RAvD5efm3NeHMEB117TYyvPUMFKbXFy8YGxRHpLyEelkA130_provenance.
- NP190194.RAvD5efm3NeHMEB117TYyvPUMFKbXFy8YGxRHpLyEelkA130_assertion evidence source_evidence_literature NP190194.RAvD5efm3NeHMEB117TYyvPUMFKbXFy8YGxRHpLyEelkA130_provenance.
- NP190194.RAvD5efm3NeHMEB117TYyvPUMFKbXFy8YGxRHpLyEelkA130_assertion SIO_000772 11889467 NP190194.RAvD5efm3NeHMEB117TYyvPUMFKbXFy8YGxRHpLyEelkA130_provenance.
- NP190194.RAvD5efm3NeHMEB117TYyvPUMFKbXFy8YGxRHpLyEelkA130_assertion wasDerivedFrom lhgdn-20090331 NP190194.RAvD5efm3NeHMEB117TYyvPUMFKbXFy8YGxRHpLyEelkA130_provenance.
- NP190194.RAvD5efm3NeHMEB117TYyvPUMFKbXFy8YGxRHpLyEelkA130_assertion wasGeneratedBy ECO_0000203 NP190194.RAvD5efm3NeHMEB117TYyvPUMFKbXFy8YGxRHpLyEelkA130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP190194.RAvD5efm3NeHMEB117TYyvPUMFKbXFy8YGxRHpLyEelkA130_provenance.