Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP224697.RAdjSH2hu46Fipay-RVGhz4EwqNg8__IfcA0_mzThPFNU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP224697.RAdjSH2hu46Fipay-RVGhz4EwqNg8__IfcA0_mzThPFNU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP224697.RAdjSH2hu46Fipay-RVGhz4EwqNg8__IfcA0_mzThPFNU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP224697.RAdjSH2hu46Fipay-RVGhz4EwqNg8__IfcA0_mzThPFNU130_provenance.
- NP224697.RAdjSH2hu46Fipay-RVGhz4EwqNg8__IfcA0_mzThPFNU130_assertion description "[We identified loss of SMARCB1 protein expression in the majority of ES cases (25/40, 62.5%), including 24/34 (71%) adult cases but only 1/6 (17%) paediatric/adolescent cases (p=0.02, two-tailed Fisher's exact test).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP224697.RAdjSH2hu46Fipay-RVGhz4EwqNg8__IfcA0_mzThPFNU130_provenance.
- NP224697.RAdjSH2hu46Fipay-RVGhz4EwqNg8__IfcA0_mzThPFNU130_assertion evidence source_evidence_literature NP224697.RAdjSH2hu46Fipay-RVGhz4EwqNg8__IfcA0_mzThPFNU130_provenance.
- NP224697.RAdjSH2hu46Fipay-RVGhz4EwqNg8__IfcA0_mzThPFNU130_assertion SIO_000772 20932739 NP224697.RAdjSH2hu46Fipay-RVGhz4EwqNg8__IfcA0_mzThPFNU130_provenance.
- NP224697.RAdjSH2hu46Fipay-RVGhz4EwqNg8__IfcA0_mzThPFNU130_assertion wasDerivedFrom befree-20140225 NP224697.RAdjSH2hu46Fipay-RVGhz4EwqNg8__IfcA0_mzThPFNU130_provenance.
- NP224697.RAdjSH2hu46Fipay-RVGhz4EwqNg8__IfcA0_mzThPFNU130_assertion wasGeneratedBy ECO_0000203 NP224697.RAdjSH2hu46Fipay-RVGhz4EwqNg8__IfcA0_mzThPFNU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP224697.RAdjSH2hu46Fipay-RVGhz4EwqNg8__IfcA0_mzThPFNU130_provenance.