Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP678420.RAv8E-yyg5-PUdgerckZd5NehgHTU0DWk2QVnHqqz3xoE130_assertion> ?p ?o ?g. }
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- NP678420.RAv8E-yyg5-PUdgerckZd5NehgHTU0DWk2QVnHqqz3xoE130_assertion type Assertion NP678420.RAv8E-yyg5-PUdgerckZd5NehgHTU0DWk2QVnHqqz3xoE130_head.
- NP678420.RAv8E-yyg5-PUdgerckZd5NehgHTU0DWk2QVnHqqz3xoE130_assertion description "[We also believe that the deletion of GPR35 could be responsible for the entity brachydactyly mental retardation syndrome (OMIM #600430), which was coined based on the above minority of patients with terminal 2q37 deletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP678420.RAv8E-yyg5-PUdgerckZd5NehgHTU0DWk2QVnHqqz3xoE130_provenance.
- NP678420.RAv8E-yyg5-PUdgerckZd5NehgHTU0DWk2QVnHqqz3xoE130_assertion evidence source_evidence_literature NP678420.RAv8E-yyg5-PUdgerckZd5NehgHTU0DWk2QVnHqqz3xoE130_provenance.
- NP678420.RAv8E-yyg5-PUdgerckZd5NehgHTU0DWk2QVnHqqz3xoE130_assertion SIO_000772 15521982 NP678420.RAv8E-yyg5-PUdgerckZd5NehgHTU0DWk2QVnHqqz3xoE130_provenance.
- NP678420.RAv8E-yyg5-PUdgerckZd5NehgHTU0DWk2QVnHqqz3xoE130_assertion wasDerivedFrom befree-20140225 NP678420.RAv8E-yyg5-PUdgerckZd5NehgHTU0DWk2QVnHqqz3xoE130_provenance.
- NP678420.RAv8E-yyg5-PUdgerckZd5NehgHTU0DWk2QVnHqqz3xoE130_assertion wasGeneratedBy ECO_0000203 NP678420.RAv8E-yyg5-PUdgerckZd5NehgHTU0DWk2QVnHqqz3xoE130_provenance.