Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP982203.RAoY3zpPD4WGMtSoB9fpZqoLrEZOmkgydibogRRTKY-Cc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP982203.RAoY3zpPD4WGMtSoB9fpZqoLrEZOmkgydibogRRTKY-Cc130_assertion type Assertion NP982203.RAoY3zpPD4WGMtSoB9fpZqoLrEZOmkgydibogRRTKY-Cc130_head.
- NP982203.RAoY3zpPD4WGMtSoB9fpZqoLrEZOmkgydibogRRTKY-Cc130_assertion description "[Mutations in the ARX gene, at Xp22.3, cause several disorders, including infantile spasms, X-linked lissencephaly with abnormal genitalia (XLAG), callosal agenesis and isolated intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP982203.RAoY3zpPD4WGMtSoB9fpZqoLrEZOmkgydibogRRTKY-Cc130_provenance.
- NP982203.RAoY3zpPD4WGMtSoB9fpZqoLrEZOmkgydibogRRTKY-Cc130_assertion evidence source_evidence_literature NP982203.RAoY3zpPD4WGMtSoB9fpZqoLrEZOmkgydibogRRTKY-Cc130_provenance.
- NP982203.RAoY3zpPD4WGMtSoB9fpZqoLrEZOmkgydibogRRTKY-Cc130_assertion SIO_000772 22585566 NP982203.RAoY3zpPD4WGMtSoB9fpZqoLrEZOmkgydibogRRTKY-Cc130_provenance.
- NP982203.RAoY3zpPD4WGMtSoB9fpZqoLrEZOmkgydibogRRTKY-Cc130_assertion wasDerivedFrom befree-2016 NP982203.RAoY3zpPD4WGMtSoB9fpZqoLrEZOmkgydibogRRTKY-Cc130_provenance.
- NP982203.RAoY3zpPD4WGMtSoB9fpZqoLrEZOmkgydibogRRTKY-Cc130_assertion wasGeneratedBy ECO_0000203 NP982203.RAoY3zpPD4WGMtSoB9fpZqoLrEZOmkgydibogRRTKY-Cc130_provenance.