Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_assertion type Assertion NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_head.
- NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_assertion description "[X-linked lissencephaly with ambiguous genitalia (XLAG) is a recently described genetic disorder caused by mutation in the aristaless-related homeobox (ARX) gene (Xp22.13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_provenance.
- NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_assertion evidence source_evidence_literature NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_provenance.
- NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_assertion SIO_000772 17221017 NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_provenance.
- NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_assertion wasDerivedFrom befree-20140225 NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_provenance.
- NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_assertion wasGeneratedBy ECO_0000203 NP744999.RA2O0lDY1U4sazByRcJtTTh133CPPFfqboJbOgkUdKuj4130_provenance.