Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP283079.RA4yW7vEDdlSAySJB8fFU_4Dnl81OuuHOsjyfeaYHMXps130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP283079.RA4yW7vEDdlSAySJB8fFU_4Dnl81OuuHOsjyfeaYHMXps130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP283079.RA4yW7vEDdlSAySJB8fFU_4Dnl81OuuHOsjyfeaYHMXps130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP283079.RA4yW7vEDdlSAySJB8fFU_4Dnl81OuuHOsjyfeaYHMXps130_provenance.
- NP283079.RA4yW7vEDdlSAySJB8fFU_4Dnl81OuuHOsjyfeaYHMXps130_assertion description "[Mutations in SRY, SOX9 and SOX10 have been shown to be responsible for XY sex reversal, campomelic dysplasia and Waardenburg-Hirschsprung disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP283079.RA4yW7vEDdlSAySJB8fFU_4Dnl81OuuHOsjyfeaYHMXps130_provenance.
- NP283079.RA4yW7vEDdlSAySJB8fFU_4Dnl81OuuHOsjyfeaYHMXps130_assertion evidence source_evidence_literature NP283079.RA4yW7vEDdlSAySJB8fFU_4Dnl81OuuHOsjyfeaYHMXps130_provenance.
- NP283079.RA4yW7vEDdlSAySJB8fFU_4Dnl81OuuHOsjyfeaYHMXps130_assertion SIO_000772 10798354 NP283079.RA4yW7vEDdlSAySJB8fFU_4Dnl81OuuHOsjyfeaYHMXps130_provenance.
- NP283079.RA4yW7vEDdlSAySJB8fFU_4Dnl81OuuHOsjyfeaYHMXps130_assertion wasDerivedFrom befree-2016 NP283079.RA4yW7vEDdlSAySJB8fFU_4Dnl81OuuHOsjyfeaYHMXps130_provenance.
- NP283079.RA4yW7vEDdlSAySJB8fFU_4Dnl81OuuHOsjyfeaYHMXps130_assertion wasGeneratedBy ECO_0000203 NP283079.RA4yW7vEDdlSAySJB8fFU_4Dnl81OuuHOsjyfeaYHMXps130_provenance.
- befree-2016 importedOn "2016-02-19" NP283079.RA4yW7vEDdlSAySJB8fFU_4Dnl81OuuHOsjyfeaYHMXps130_provenance.