Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP98961.RAfDpRsHJbyVXhfap8onoy0reG-DVmKN1NYDsanfFCC5c130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP98961.RAfDpRsHJbyVXhfap8onoy0reG-DVmKN1NYDsanfFCC5c130_assertion type Assertion NP98961.RAfDpRsHJbyVXhfap8onoy0reG-DVmKN1NYDsanfFCC5c130_head.
- NP98961.RAfDpRsHJbyVXhfap8onoy0reG-DVmKN1NYDsanfFCC5c130_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." NP98961.RAfDpRsHJbyVXhfap8onoy0reG-DVmKN1NYDsanfFCC5c130_provenance.
- NP98961.RAfDpRsHJbyVXhfap8onoy0reG-DVmKN1NYDsanfFCC5c130_assertion evidence source_evidence_literature NP98961.RAfDpRsHJbyVXhfap8onoy0reG-DVmKN1NYDsanfFCC5c130_provenance.
- NP98961.RAfDpRsHJbyVXhfap8onoy0reG-DVmKN1NYDsanfFCC5c130_assertion SIO_000772 18975239 NP98961.RAfDpRsHJbyVXhfap8onoy0reG-DVmKN1NYDsanfFCC5c130_provenance.
- NP98961.RAfDpRsHJbyVXhfap8onoy0reG-DVmKN1NYDsanfFCC5c130_assertion wasDerivedFrom lhgdn-20090331 NP98961.RAfDpRsHJbyVXhfap8onoy0reG-DVmKN1NYDsanfFCC5c130_provenance.
- NP98961.RAfDpRsHJbyVXhfap8onoy0reG-DVmKN1NYDsanfFCC5c130_assertion wasGeneratedBy ECO_0000203 NP98961.RAfDpRsHJbyVXhfap8onoy0reG-DVmKN1NYDsanfFCC5c130_provenance.