Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP301394.RAkkWf8ocGksTGwI_r7dH0VopcRS3IDLtPbN6SBjNbRgU130_assertion> ?p ?o ?g. }
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- NP301394.RAkkWf8ocGksTGwI_r7dH0VopcRS3IDLtPbN6SBjNbRgU130_assertion type Assertion NP301394.RAkkWf8ocGksTGwI_r7dH0VopcRS3IDLtPbN6SBjNbRgU130_head.
- NP301394.RAkkWf8ocGksTGwI_r7dH0VopcRS3IDLtPbN6SBjNbRgU130_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." NP301394.RAkkWf8ocGksTGwI_r7dH0VopcRS3IDLtPbN6SBjNbRgU130_provenance.
- NP301394.RAkkWf8ocGksTGwI_r7dH0VopcRS3IDLtPbN6SBjNbRgU130_assertion evidence source_evidence_literature NP301394.RAkkWf8ocGksTGwI_r7dH0VopcRS3IDLtPbN6SBjNbRgU130_provenance.
- NP301394.RAkkWf8ocGksTGwI_r7dH0VopcRS3IDLtPbN6SBjNbRgU130_assertion SIO_000772 10982188 NP301394.RAkkWf8ocGksTGwI_r7dH0VopcRS3IDLtPbN6SBjNbRgU130_provenance.
- NP301394.RAkkWf8ocGksTGwI_r7dH0VopcRS3IDLtPbN6SBjNbRgU130_assertion wasDerivedFrom befree-20140225 NP301394.RAkkWf8ocGksTGwI_r7dH0VopcRS3IDLtPbN6SBjNbRgU130_provenance.
- NP301394.RAkkWf8ocGksTGwI_r7dH0VopcRS3IDLtPbN6SBjNbRgU130_assertion wasGeneratedBy ECO_0000203 NP301394.RAkkWf8ocGksTGwI_r7dH0VopcRS3IDLtPbN6SBjNbRgU130_provenance.