Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP189985.RAFQomXe_fv9uutNtqbaeg_lPQIvqI30fD7-KzWJcX_GY130_assertion> ?p ?o ?g. }
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- NP189985.RAFQomXe_fv9uutNtqbaeg_lPQIvqI30fD7-KzWJcX_GY130_assertion type Assertion NP189985.RAFQomXe_fv9uutNtqbaeg_lPQIvqI30fD7-KzWJcX_GY130_head.
- NP189985.RAFQomXe_fv9uutNtqbaeg_lPQIvqI30fD7-KzWJcX_GY130_assertion wasGeneratedBy ECO_0000203 NP189985.RAFQomXe_fv9uutNtqbaeg_lPQIvqI30fD7-KzWJcX_GY130_provenance.
- NP189985.RAFQomXe_fv9uutNtqbaeg_lPQIvqI30fD7-KzWJcX_GY130_assertion wasDerivedFrom lhgdn-20090331 NP189985.RAFQomXe_fv9uutNtqbaeg_lPQIvqI30fD7-KzWJcX_GY130_provenance.
- NP189985.RAFQomXe_fv9uutNtqbaeg_lPQIvqI30fD7-KzWJcX_GY130_assertion SIO_000772 12838518 NP189985.RAFQomXe_fv9uutNtqbaeg_lPQIvqI30fD7-KzWJcX_GY130_provenance.
- NP189985.RAFQomXe_fv9uutNtqbaeg_lPQIvqI30fD7-KzWJcX_GY130_assertion evidence source_evidence_literature NP189985.RAFQomXe_fv9uutNtqbaeg_lPQIvqI30fD7-KzWJcX_GY130_provenance.
- NP189985.RAFQomXe_fv9uutNtqbaeg_lPQIvqI30fD7-KzWJcX_GY130_assertion description "[Missense DCX mutations may manifest as non-syndromic mental retardation with cryptogenic epilepsy in female subjects and subcortical band heterotopia (SBH) in boys.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP189985.RAFQomXe_fv9uutNtqbaeg_lPQIvqI30fD7-KzWJcX_GY130_provenance.