Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP401184.RAzOCKlinG8ZSfgsr-Ag3dk89YpwVwtM2FYYtdeGdpYBc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP401184.RAzOCKlinG8ZSfgsr-Ag3dk89YpwVwtM2FYYtdeGdpYBc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP401184.RAzOCKlinG8ZSfgsr-Ag3dk89YpwVwtM2FYYtdeGdpYBc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP401184.RAzOCKlinG8ZSfgsr-Ag3dk89YpwVwtM2FYYtdeGdpYBc130_provenance.
- NP401184.RAzOCKlinG8ZSfgsr-Ag3dk89YpwVwtM2FYYtdeGdpYBc130_assertion description "[Moreover, as mutations of the SOX10 transcription factor were previously described in Waardenburg-Hirschsprung disease, these results show that SOX10 mutations cause various types of neurocristopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401184.RAzOCKlinG8ZSfgsr-Ag3dk89YpwVwtM2FYYtdeGdpYBc130_provenance.
- NP401184.RAzOCKlinG8ZSfgsr-Ag3dk89YpwVwtM2FYYtdeGdpYBc130_assertion evidence source_evidence_literature NP401184.RAzOCKlinG8ZSfgsr-Ag3dk89YpwVwtM2FYYtdeGdpYBc130_provenance.
- NP401184.RAzOCKlinG8ZSfgsr-Ag3dk89YpwVwtM2FYYtdeGdpYBc130_assertion SIO_000772 10441344 NP401184.RAzOCKlinG8ZSfgsr-Ag3dk89YpwVwtM2FYYtdeGdpYBc130_provenance.
- NP401184.RAzOCKlinG8ZSfgsr-Ag3dk89YpwVwtM2FYYtdeGdpYBc130_assertion wasDerivedFrom befree-20140225 NP401184.RAzOCKlinG8ZSfgsr-Ag3dk89YpwVwtM2FYYtdeGdpYBc130_provenance.
- NP401184.RAzOCKlinG8ZSfgsr-Ag3dk89YpwVwtM2FYYtdeGdpYBc130_assertion wasGeneratedBy ECO_0000203 NP401184.RAzOCKlinG8ZSfgsr-Ag3dk89YpwVwtM2FYYtdeGdpYBc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP401184.RAzOCKlinG8ZSfgsr-Ag3dk89YpwVwtM2FYYtdeGdpYBc130_provenance.