Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP284036.RAcETkKhDor2fi9gKQdLbnA7_9nuQK3ckEWbzbYYldXxA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP284036.RAcETkKhDor2fi9gKQdLbnA7_9nuQK3ckEWbzbYYldXxA130_assertion type Assertion NP284036.RAcETkKhDor2fi9gKQdLbnA7_9nuQK3ckEWbzbYYldXxA130_head.
- NP284036.RAcETkKhDor2fi9gKQdLbnA7_9nuQK3ckEWbzbYYldXxA130_assertion wasGeneratedBy ECO_0000203 NP284036.RAcETkKhDor2fi9gKQdLbnA7_9nuQK3ckEWbzbYYldXxA130_provenance.
- NP284036.RAcETkKhDor2fi9gKQdLbnA7_9nuQK3ckEWbzbYYldXxA130_assertion wasDerivedFrom befree-20140225 NP284036.RAcETkKhDor2fi9gKQdLbnA7_9nuQK3ckEWbzbYYldXxA130_provenance.
- NP284036.RAcETkKhDor2fi9gKQdLbnA7_9nuQK3ckEWbzbYYldXxA130_assertion SIO_000772 9615224 NP284036.RAcETkKhDor2fi9gKQdLbnA7_9nuQK3ckEWbzbYYldXxA130_provenance.
- NP284036.RAcETkKhDor2fi9gKQdLbnA7_9nuQK3ckEWbzbYYldXxA130_assertion evidence source_evidence_literature NP284036.RAcETkKhDor2fi9gKQdLbnA7_9nuQK3ckEWbzbYYldXxA130_provenance.
- NP284036.RAcETkKhDor2fi9gKQdLbnA7_9nuQK3ckEWbzbYYldXxA130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284036.RAcETkKhDor2fi9gKQdLbnA7_9nuQK3ckEWbzbYYldXxA130_provenance.