Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_assertion type Assertion NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_head.
- NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_assertion description "[X-linked lissencephaly with abnormal genitalia (XLAG) is a rare disorder caused by mutations in the aristaless-related homeobox (ARX) gene, located on Xp22.13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_provenance.
- NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_assertion evidence source_evidence_literature NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_provenance.
- NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_assertion SIO_000772 18458920 NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_provenance.
- NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_assertion wasDerivedFrom befree-20150227 NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_provenance.
- NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_assertion wasGeneratedBy ECO_0000203 NP978176.RAoh10r_0JX6JEFfIxD3qtfqF1qYGtlI5JwjoaFz5VApo130_provenance.