Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP457263.RAP_9ink73_JFRAUqX1FlZQgalfCYLE6MvYaFy-SwT3CU130_assertion> ?p ?o ?g. }
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- NP457263.RAP_9ink73_JFRAUqX1FlZQgalfCYLE6MvYaFy-SwT3CU130_assertion type Assertion NP457263.RAP_9ink73_JFRAUqX1FlZQgalfCYLE6MvYaFy-SwT3CU130_head.
- NP457263.RAP_9ink73_JFRAUqX1FlZQgalfCYLE6MvYaFy-SwT3CU130_assertion description "[However, in one family (MRX19), a missense mutation was associated solely with mild mental retardation and no other clinical feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP457263.RAP_9ink73_JFRAUqX1FlZQgalfCYLE6MvYaFy-SwT3CU130_provenance.
- NP457263.RAP_9ink73_JFRAUqX1FlZQgalfCYLE6MvYaFy-SwT3CU130_assertion evidence source_evidence_literature NP457263.RAP_9ink73_JFRAUqX1FlZQgalfCYLE6MvYaFy-SwT3CU130_provenance.
- NP457263.RAP_9ink73_JFRAUqX1FlZQgalfCYLE6MvYaFy-SwT3CU130_assertion SIO_000772 11896450 NP457263.RAP_9ink73_JFRAUqX1FlZQgalfCYLE6MvYaFy-SwT3CU130_provenance.
- NP457263.RAP_9ink73_JFRAUqX1FlZQgalfCYLE6MvYaFy-SwT3CU130_assertion wasDerivedFrom befree-20140225 NP457263.RAP_9ink73_JFRAUqX1FlZQgalfCYLE6MvYaFy-SwT3CU130_provenance.
- NP457263.RAP_9ink73_JFRAUqX1FlZQgalfCYLE6MvYaFy-SwT3CU130_assertion wasGeneratedBy ECO_0000203 NP457263.RAP_9ink73_JFRAUqX1FlZQgalfCYLE6MvYaFy-SwT3CU130_provenance.