Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP844312.RADduLtV1xfO6cJeofCd5MMZLhqNDJ5PBlzAaUS2tnFqk130_assertion> ?p ?o ?g. }
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- NP844312.RADduLtV1xfO6cJeofCd5MMZLhqNDJ5PBlzAaUS2tnFqk130_assertion type Assertion NP844312.RADduLtV1xfO6cJeofCd5MMZLhqNDJ5PBlzAaUS2tnFqk130_head.
- NP844312.RADduLtV1xfO6cJeofCd5MMZLhqNDJ5PBlzAaUS2tnFqk130_assertion description "[Mutations in SLC9A6 are associated with Christianson syndrome (OMIM 300243), a syndromic form of X-linked mental retardation (XLMR) characterized by microcephaly, severe global developmental delay, ataxia and seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP844312.RADduLtV1xfO6cJeofCd5MMZLhqNDJ5PBlzAaUS2tnFqk130_provenance.
- NP844312.RADduLtV1xfO6cJeofCd5MMZLhqNDJ5PBlzAaUS2tnFqk130_assertion evidence source_evidence_literature NP844312.RADduLtV1xfO6cJeofCd5MMZLhqNDJ5PBlzAaUS2tnFqk130_provenance.
- NP844312.RADduLtV1xfO6cJeofCd5MMZLhqNDJ5PBlzAaUS2tnFqk130_assertion SIO_000772 21932316 NP844312.RADduLtV1xfO6cJeofCd5MMZLhqNDJ5PBlzAaUS2tnFqk130_provenance.
- NP844312.RADduLtV1xfO6cJeofCd5MMZLhqNDJ5PBlzAaUS2tnFqk130_assertion wasDerivedFrom befree-20150227 NP844312.RADduLtV1xfO6cJeofCd5MMZLhqNDJ5PBlzAaUS2tnFqk130_provenance.
- NP844312.RADduLtV1xfO6cJeofCd5MMZLhqNDJ5PBlzAaUS2tnFqk130_assertion wasGeneratedBy ECO_0000203 NP844312.RADduLtV1xfO6cJeofCd5MMZLhqNDJ5PBlzAaUS2tnFqk130_provenance.