Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_assertion> ?p ?o ?g. }
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- NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_assertion type Assertion NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_head.
- NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_assertion wasGeneratedBy ECO_0000203 NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_provenance.
- NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_assertion wasDerivedFrom befree-20150227 NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_provenance.
- NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_assertion SIO_000772 9615224 NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_provenance.
- NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_assertion evidence source_evidence_literature NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_provenance.
- NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_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." NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_provenance.