Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP243311.RAgLMH7z1oa5YANxq-XL0bcYPJ-0pvfHeVwJMME2YTb4M130_assertion> ?p ?o ?g. }
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- NP243311.RAgLMH7z1oa5YANxq-XL0bcYPJ-0pvfHeVwJMME2YTb4M130_assertion type Assertion NP243311.RAgLMH7z1oa5YANxq-XL0bcYPJ-0pvfHeVwJMME2YTb4M130_head.
- NP243311.RAgLMH7z1oa5YANxq-XL0bcYPJ-0pvfHeVwJMME2YTb4M130_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." NP243311.RAgLMH7z1oa5YANxq-XL0bcYPJ-0pvfHeVwJMME2YTb4M130_provenance.
- NP243311.RAgLMH7z1oa5YANxq-XL0bcYPJ-0pvfHeVwJMME2YTb4M130_assertion evidence source_evidence_literature NP243311.RAgLMH7z1oa5YANxq-XL0bcYPJ-0pvfHeVwJMME2YTb4M130_provenance.
- NP243311.RAgLMH7z1oa5YANxq-XL0bcYPJ-0pvfHeVwJMME2YTb4M130_assertion SIO_000772 18975239 NP243311.RAgLMH7z1oa5YANxq-XL0bcYPJ-0pvfHeVwJMME2YTb4M130_provenance.
- NP243311.RAgLMH7z1oa5YANxq-XL0bcYPJ-0pvfHeVwJMME2YTb4M130_assertion wasDerivedFrom lhgdn-20090331 NP243311.RAgLMH7z1oa5YANxq-XL0bcYPJ-0pvfHeVwJMME2YTb4M130_provenance.
- NP243311.RAgLMH7z1oa5YANxq-XL0bcYPJ-0pvfHeVwJMME2YTb4M130_assertion wasGeneratedBy ECO_0000203 NP243311.RAgLMH7z1oa5YANxq-XL0bcYPJ-0pvfHeVwJMME2YTb4M130_provenance.