Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_assertion> ?p ?o ?g. }
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- NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_assertion type Assertion NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_head.
- NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_assertion description "[Disorders caused by mutations in the ARX gene include: hydrocephaly, lissencephaly and agenesis of corpus callosum with abnormal genitalia, Partington syndrome S), X-linked infantile spasms, myoclonic epilepsy, and nonspecific mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_provenance.
- NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_assertion evidence source_evidence_literature NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_provenance.
- NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_assertion SIO_000772 18975239 NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_provenance.
- NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_assertion wasDerivedFrom lhgdn-20090331 NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_provenance.
- NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_assertion wasGeneratedBy ECO_0000203 NP147703.RAXSML0u9a7IYoYNcs6PfLsIp2BWk62cCsdJY03X7Tc_o130_provenance.