Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP957742.RA_rqEgsWHZhc-k142qOgyLt2o466vbs6CuragfQ29_pE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP957742.RA_rqEgsWHZhc-k142qOgyLt2o466vbs6CuragfQ29_pE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP957742.RA_rqEgsWHZhc-k142qOgyLt2o466vbs6CuragfQ29_pE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP957742.RA_rqEgsWHZhc-k142qOgyLt2o466vbs6CuragfQ29_pE130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP957742.RA_rqEgsWHZhc-k142qOgyLt2o466vbs6CuragfQ29_pE130_provenance.