Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP844312.RADduLtV1xfO6cJeofCd5MMZLhqNDJ5PBlzAaUS2tnFqk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP844312.RADduLtV1xfO6cJeofCd5MMZLhqNDJ5PBlzAaUS2tnFqk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP844312.RADduLtV1xfO6cJeofCd5MMZLhqNDJ5PBlzAaUS2tnFqk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP844312.RADduLtV1xfO6cJeofCd5MMZLhqNDJ5PBlzAaUS2tnFqk130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP844312.RADduLtV1xfO6cJeofCd5MMZLhqNDJ5PBlzAaUS2tnFqk130_provenance.