Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978103.RANLq4Ht-3v5a98HUfCe9P1By7Pj0Q4L3pnQpV0ERZvZQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP978103.RANLq4Ht-3v5a98HUfCe9P1By7Pj0Q4L3pnQpV0ERZvZQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978103.RANLq4Ht-3v5a98HUfCe9P1By7Pj0Q4L3pnQpV0ERZvZQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978103.RANLq4Ht-3v5a98HUfCe9P1By7Pj0Q4L3pnQpV0ERZvZQ130_provenance.
- NP978103.RANLq4Ht-3v5a98HUfCe9P1By7Pj0Q4L3pnQpV0ERZvZQ130_assertion description "[Mutations in the Aristaless-related homeobox (ARX) gene are associated with pleiotropic phenotypes including infantile spasms, mental retardation and dystonia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978103.RANLq4Ht-3v5a98HUfCe9P1By7Pj0Q4L3pnQpV0ERZvZQ130_provenance.
- NP978103.RANLq4Ht-3v5a98HUfCe9P1By7Pj0Q4L3pnQpV0ERZvZQ130_assertion evidence source_evidence_literature NP978103.RANLq4Ht-3v5a98HUfCe9P1By7Pj0Q4L3pnQpV0ERZvZQ130_provenance.
- NP978103.RANLq4Ht-3v5a98HUfCe9P1By7Pj0Q4L3pnQpV0ERZvZQ130_assertion SIO_000772 18823727 NP978103.RANLq4Ht-3v5a98HUfCe9P1By7Pj0Q4L3pnQpV0ERZvZQ130_provenance.
- NP978103.RANLq4Ht-3v5a98HUfCe9P1By7Pj0Q4L3pnQpV0ERZvZQ130_assertion wasDerivedFrom befree-20150227 NP978103.RANLq4Ht-3v5a98HUfCe9P1By7Pj0Q4L3pnQpV0ERZvZQ130_provenance.
- NP978103.RANLq4Ht-3v5a98HUfCe9P1By7Pj0Q4L3pnQpV0ERZvZQ130_assertion wasGeneratedBy ECO_0000203 NP978103.RANLq4Ht-3v5a98HUfCe9P1By7Pj0Q4L3pnQpV0ERZvZQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978103.RANLq4Ht-3v5a98HUfCe9P1By7Pj0Q4L3pnQpV0ERZvZQ130_provenance.