Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP294751.RAgXQeIG29xk5hx-S76gdt8VpnwUwEAzWe4XBS9h45fRE130_assertion> ?p ?o ?g. }
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- NP294751.RAgXQeIG29xk5hx-S76gdt8VpnwUwEAzWe4XBS9h45fRE130_assertion type Assertion NP294751.RAgXQeIG29xk5hx-S76gdt8VpnwUwEAzWe4XBS9h45fRE130_head.
- NP294751.RAgXQeIG29xk5hx-S76gdt8VpnwUwEAzWe4XBS9h45fRE130_assertion description "[Small ring (X) chromosomes lacking the XIST gene at Xq13.2 have been associated with a severe phenotype that includes mental retardation, facial dysmorphism and congenital abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294751.RAgXQeIG29xk5hx-S76gdt8VpnwUwEAzWe4XBS9h45fRE130_provenance.
- NP294751.RAgXQeIG29xk5hx-S76gdt8VpnwUwEAzWe4XBS9h45fRE130_assertion evidence source_evidence_literature NP294751.RAgXQeIG29xk5hx-S76gdt8VpnwUwEAzWe4XBS9h45fRE130_provenance.
- NP294751.RAgXQeIG29xk5hx-S76gdt8VpnwUwEAzWe4XBS9h45fRE130_assertion SIO_000772 10982188 NP294751.RAgXQeIG29xk5hx-S76gdt8VpnwUwEAzWe4XBS9h45fRE130_provenance.
- NP294751.RAgXQeIG29xk5hx-S76gdt8VpnwUwEAzWe4XBS9h45fRE130_assertion wasDerivedFrom befree-2016 NP294751.RAgXQeIG29xk5hx-S76gdt8VpnwUwEAzWe4XBS9h45fRE130_provenance.
- NP294751.RAgXQeIG29xk5hx-S76gdt8VpnwUwEAzWe4XBS9h45fRE130_assertion wasGeneratedBy ECO_0000203 NP294751.RAgXQeIG29xk5hx-S76gdt8VpnwUwEAzWe4XBS9h45fRE130_provenance.