Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP416899.RAw5wdSx1-lFbpp_3uUsp2vH6BMY924cbtrhqlyJnv7bs130_assertion> ?p ?o ?g. }
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- NP416899.RAw5wdSx1-lFbpp_3uUsp2vH6BMY924cbtrhqlyJnv7bs130_assertion type Assertion NP416899.RAw5wdSx1-lFbpp_3uUsp2vH6BMY924cbtrhqlyJnv7bs130_head.
- NP416899.RAw5wdSx1-lFbpp_3uUsp2vH6BMY924cbtrhqlyJnv7bs130_assertion wasGeneratedBy ECO_0000203 NP416899.RAw5wdSx1-lFbpp_3uUsp2vH6BMY924cbtrhqlyJnv7bs130_provenance.
- NP416899.RAw5wdSx1-lFbpp_3uUsp2vH6BMY924cbtrhqlyJnv7bs130_assertion wasDerivedFrom befree-20140225 NP416899.RAw5wdSx1-lFbpp_3uUsp2vH6BMY924cbtrhqlyJnv7bs130_provenance.
- NP416899.RAw5wdSx1-lFbpp_3uUsp2vH6BMY924cbtrhqlyJnv7bs130_assertion SIO_000772 9615224 NP416899.RAw5wdSx1-lFbpp_3uUsp2vH6BMY924cbtrhqlyJnv7bs130_provenance.
- NP416899.RAw5wdSx1-lFbpp_3uUsp2vH6BMY924cbtrhqlyJnv7bs130_assertion evidence source_evidence_literature NP416899.RAw5wdSx1-lFbpp_3uUsp2vH6BMY924cbtrhqlyJnv7bs130_provenance.
- NP416899.RAw5wdSx1-lFbpp_3uUsp2vH6BMY924cbtrhqlyJnv7bs130_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." NP416899.RAw5wdSx1-lFbpp_3uUsp2vH6BMY924cbtrhqlyJnv7bs130_provenance.