Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP496801.RArU3JUk1ptE3JYa9D88ZSWv54p1pFXNJ4AWiTykTGMFk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP496801.RArU3JUk1ptE3JYa9D88ZSWv54p1pFXNJ4AWiTykTGMFk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP496801.RArU3JUk1ptE3JYa9D88ZSWv54p1pFXNJ4AWiTykTGMFk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP496801.RArU3JUk1ptE3JYa9D88ZSWv54p1pFXNJ4AWiTykTGMFk130_provenance.
- NP496801.RArU3JUk1ptE3JYa9D88ZSWv54p1pFXNJ4AWiTykTGMFk130_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." NP496801.RArU3JUk1ptE3JYa9D88ZSWv54p1pFXNJ4AWiTykTGMFk130_provenance.
- NP496801.RArU3JUk1ptE3JYa9D88ZSWv54p1pFXNJ4AWiTykTGMFk130_assertion evidence source_evidence_literature NP496801.RArU3JUk1ptE3JYa9D88ZSWv54p1pFXNJ4AWiTykTGMFk130_provenance.
- NP496801.RArU3JUk1ptE3JYa9D88ZSWv54p1pFXNJ4AWiTykTGMFk130_assertion SIO_000772 15921244 NP496801.RArU3JUk1ptE3JYa9D88ZSWv54p1pFXNJ4AWiTykTGMFk130_provenance.
- NP496801.RArU3JUk1ptE3JYa9D88ZSWv54p1pFXNJ4AWiTykTGMFk130_assertion wasDerivedFrom befree-2016 NP496801.RArU3JUk1ptE3JYa9D88ZSWv54p1pFXNJ4AWiTykTGMFk130_provenance.
- NP496801.RArU3JUk1ptE3JYa9D88ZSWv54p1pFXNJ4AWiTykTGMFk130_assertion wasGeneratedBy ECO_0000203 NP496801.RArU3JUk1ptE3JYa9D88ZSWv54p1pFXNJ4AWiTykTGMFk130_provenance.
- befree-2016 importedOn "2016-02-19" NP496801.RArU3JUk1ptE3JYa9D88ZSWv54p1pFXNJ4AWiTykTGMFk130_provenance.