Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP778971.RAiWGtSyfoLxdnzLFKP_4lZHN1lqJS_p_rCYbrH2kWb4U130_assertion> ?p ?o ?g. }
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- NP778971.RAiWGtSyfoLxdnzLFKP_4lZHN1lqJS_p_rCYbrH2kWb4U130_assertion type Assertion NP778971.RAiWGtSyfoLxdnzLFKP_4lZHN1lqJS_p_rCYbrH2kWb4U130_head.
- NP778971.RAiWGtSyfoLxdnzLFKP_4lZHN1lqJS_p_rCYbrH2kWb4U130_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." NP778971.RAiWGtSyfoLxdnzLFKP_4lZHN1lqJS_p_rCYbrH2kWb4U130_provenance.
- NP778971.RAiWGtSyfoLxdnzLFKP_4lZHN1lqJS_p_rCYbrH2kWb4U130_assertion evidence source_evidence_literature NP778971.RAiWGtSyfoLxdnzLFKP_4lZHN1lqJS_p_rCYbrH2kWb4U130_provenance.
- NP778971.RAiWGtSyfoLxdnzLFKP_4lZHN1lqJS_p_rCYbrH2kWb4U130_assertion SIO_000772 10982188 NP778971.RAiWGtSyfoLxdnzLFKP_4lZHN1lqJS_p_rCYbrH2kWb4U130_provenance.
- NP778971.RAiWGtSyfoLxdnzLFKP_4lZHN1lqJS_p_rCYbrH2kWb4U130_assertion wasDerivedFrom befree-20150227 NP778971.RAiWGtSyfoLxdnzLFKP_4lZHN1lqJS_p_rCYbrH2kWb4U130_provenance.
- NP778971.RAiWGtSyfoLxdnzLFKP_4lZHN1lqJS_p_rCYbrH2kWb4U130_assertion wasGeneratedBy ECO_0000203 NP778971.RAiWGtSyfoLxdnzLFKP_4lZHN1lqJS_p_rCYbrH2kWb4U130_provenance.