Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP957742.RA_rqEgsWHZhc-k142qOgyLt2o466vbs6CuragfQ29_pE130_assertion> ?p ?o ?g. }
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- NP957742.RA_rqEgsWHZhc-k142qOgyLt2o466vbs6CuragfQ29_pE130_assertion type Assertion NP957742.RA_rqEgsWHZhc-k142qOgyLt2o466vbs6CuragfQ29_pE130_head.
- NP957742.RA_rqEgsWHZhc-k142qOgyLt2o466vbs6CuragfQ29_pE130_assertion description "[This patient broadens the spectrum of SLC9A6 mutations and contributes to the clinical delineation of Christianson syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP957742.RA_rqEgsWHZhc-k142qOgyLt2o466vbs6CuragfQ29_pE130_provenance.
- NP957742.RA_rqEgsWHZhc-k142qOgyLt2o466vbs6CuragfQ29_pE130_assertion evidence source_evidence_literature NP957742.RA_rqEgsWHZhc-k142qOgyLt2o466vbs6CuragfQ29_pE130_provenance.
- NP957742.RA_rqEgsWHZhc-k142qOgyLt2o466vbs6CuragfQ29_pE130_assertion SIO_000772 21932316 NP957742.RA_rqEgsWHZhc-k142qOgyLt2o466vbs6CuragfQ29_pE130_provenance.
- NP957742.RA_rqEgsWHZhc-k142qOgyLt2o466vbs6CuragfQ29_pE130_assertion wasDerivedFrom befree-20150227 NP957742.RA_rqEgsWHZhc-k142qOgyLt2o466vbs6CuragfQ29_pE130_provenance.
- NP957742.RA_rqEgsWHZhc-k142qOgyLt2o466vbs6CuragfQ29_pE130_assertion wasGeneratedBy ECO_0000203 NP957742.RA_rqEgsWHZhc-k142qOgyLt2o466vbs6CuragfQ29_pE130_provenance.