Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP496800.RAJkOP7CbnkgNHpYmFzgD4SlqphGZdTAHhd5XorKSWAdg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP496800.RAJkOP7CbnkgNHpYmFzgD4SlqphGZdTAHhd5XorKSWAdg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP496800.RAJkOP7CbnkgNHpYmFzgD4SlqphGZdTAHhd5XorKSWAdg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP496800.RAJkOP7CbnkgNHpYmFzgD4SlqphGZdTAHhd5XorKSWAdg130_provenance.
- NP496800.RAJkOP7CbnkgNHpYmFzgD4SlqphGZdTAHhd5XorKSWAdg130_assertion description "[The striking epileptogenicity of X-linked lissencephaly with abnormal genitalia and West's syndrome associated with ARX mutations i s considered to be caused by a disorder of interneurons involving a tangentialmigration disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP496800.RAJkOP7CbnkgNHpYmFzgD4SlqphGZdTAHhd5XorKSWAdg130_provenance.
- NP496800.RAJkOP7CbnkgNHpYmFzgD4SlqphGZdTAHhd5XorKSWAdg130_assertion evidence source_evidence_literature NP496800.RAJkOP7CbnkgNHpYmFzgD4SlqphGZdTAHhd5XorKSWAdg130_provenance.
- NP496800.RAJkOP7CbnkgNHpYmFzgD4SlqphGZdTAHhd5XorKSWAdg130_assertion SIO_000772 15921244 NP496800.RAJkOP7CbnkgNHpYmFzgD4SlqphGZdTAHhd5XorKSWAdg130_provenance.
- NP496800.RAJkOP7CbnkgNHpYmFzgD4SlqphGZdTAHhd5XorKSWAdg130_assertion wasDerivedFrom befree-2016 NP496800.RAJkOP7CbnkgNHpYmFzgD4SlqphGZdTAHhd5XorKSWAdg130_provenance.
- NP496800.RAJkOP7CbnkgNHpYmFzgD4SlqphGZdTAHhd5XorKSWAdg130_assertion wasGeneratedBy ECO_0000203 NP496800.RAJkOP7CbnkgNHpYmFzgD4SlqphGZdTAHhd5XorKSWAdg130_provenance.
- befree-2016 importedOn "2016-02-19" NP496800.RAJkOP7CbnkgNHpYmFzgD4SlqphGZdTAHhd5XorKSWAdg130_provenance.