Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP802318.RAzJSrbb2G9S2SJOY8DhyX3GCq2SVUuw-vS0tSA_Fl5aA130_assertion> ?p ?o ?g. }
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- NP802318.RAzJSrbb2G9S2SJOY8DhyX3GCq2SVUuw-vS0tSA_Fl5aA130_assertion type Assertion NP802318.RAzJSrbb2G9S2SJOY8DhyX3GCq2SVUuw-vS0tSA_Fl5aA130_head.
- NP802318.RAzJSrbb2G9S2SJOY8DhyX3GCq2SVUuw-vS0tSA_Fl5aA130_assertion description "[Cohen syndrome is an autosomal recessive, multiple congenital anomalies/mental retardation (MCA/MR) syndrome, caused by a mutation in the COH1 gen, localized on chromosome 8q22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802318.RAzJSrbb2G9S2SJOY8DhyX3GCq2SVUuw-vS0tSA_Fl5aA130_provenance.
- NP802318.RAzJSrbb2G9S2SJOY8DhyX3GCq2SVUuw-vS0tSA_Fl5aA130_assertion evidence source_evidence_literature NP802318.RAzJSrbb2G9S2SJOY8DhyX3GCq2SVUuw-vS0tSA_Fl5aA130_provenance.
- NP802318.RAzJSrbb2G9S2SJOY8DhyX3GCq2SVUuw-vS0tSA_Fl5aA130_assertion SIO_000772 18564496 NP802318.RAzJSrbb2G9S2SJOY8DhyX3GCq2SVUuw-vS0tSA_Fl5aA130_provenance.
- NP802318.RAzJSrbb2G9S2SJOY8DhyX3GCq2SVUuw-vS0tSA_Fl5aA130_assertion wasDerivedFrom befree-20140225 NP802318.RAzJSrbb2G9S2SJOY8DhyX3GCq2SVUuw-vS0tSA_Fl5aA130_provenance.
- NP802318.RAzJSrbb2G9S2SJOY8DhyX3GCq2SVUuw-vS0tSA_Fl5aA130_assertion wasGeneratedBy ECO_0000203 NP802318.RAzJSrbb2G9S2SJOY8DhyX3GCq2SVUuw-vS0tSA_Fl5aA130_provenance.