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- NP438330.RAJvApbQWWOBm78ceTOZJMw1RrFEZk6H6aAaIppmW-Z_U130_assertion type Assertion NP438330.RAJvApbQWWOBm78ceTOZJMw1RrFEZk6H6aAaIppmW-Z_U130_head.
- NP438330.RAJvApbQWWOBm78ceTOZJMw1RrFEZk6H6aAaIppmW-Z_U130_assertion wasGeneratedBy ECO_0000203 NP438330.RAJvApbQWWOBm78ceTOZJMw1RrFEZk6H6aAaIppmW-Z_U130_provenance.
- NP438330.RAJvApbQWWOBm78ceTOZJMw1RrFEZk6H6aAaIppmW-Z_U130_assertion wasDerivedFrom befree-20140225 NP438330.RAJvApbQWWOBm78ceTOZJMw1RrFEZk6H6aAaIppmW-Z_U130_provenance.
- NP438330.RAJvApbQWWOBm78ceTOZJMw1RrFEZk6H6aAaIppmW-Z_U130_assertion SIO_000772 9615224 NP438330.RAJvApbQWWOBm78ceTOZJMw1RrFEZk6H6aAaIppmW-Z_U130_provenance.
- NP438330.RAJvApbQWWOBm78ceTOZJMw1RrFEZk6H6aAaIppmW-Z_U130_assertion evidence source_evidence_literature NP438330.RAJvApbQWWOBm78ceTOZJMw1RrFEZk6H6aAaIppmW-Z_U130_provenance.
- NP438330.RAJvApbQWWOBm78ceTOZJMw1RrFEZk6H6aAaIppmW-Z_U130_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." NP438330.RAJvApbQWWOBm78ceTOZJMw1RrFEZk6H6aAaIppmW-Z_U130_provenance.