Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP435576.RAVfV2MRB8L6aKhISigIwhn9_G2XS6mxjxOHygIEhJdUU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP435576.RAVfV2MRB8L6aKhISigIwhn9_G2XS6mxjxOHygIEhJdUU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP435576.RAVfV2MRB8L6aKhISigIwhn9_G2XS6mxjxOHygIEhJdUU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP435576.RAVfV2MRB8L6aKhISigIwhn9_G2XS6mxjxOHygIEhJdUU130_provenance.
- NP435576.RAVfV2MRB8L6aKhISigIwhn9_G2XS6mxjxOHygIEhJdUU130_assertion wasGeneratedBy ECO_0000203 NP435576.RAVfV2MRB8L6aKhISigIwhn9_G2XS6mxjxOHygIEhJdUU130_provenance.
- NP435576.RAVfV2MRB8L6aKhISigIwhn9_G2XS6mxjxOHygIEhJdUU130_assertion wasDerivedFrom befree-20140225 NP435576.RAVfV2MRB8L6aKhISigIwhn9_G2XS6mxjxOHygIEhJdUU130_provenance.
- NP435576.RAVfV2MRB8L6aKhISigIwhn9_G2XS6mxjxOHygIEhJdUU130_assertion SIO_000772 20130826 NP435576.RAVfV2MRB8L6aKhISigIwhn9_G2XS6mxjxOHygIEhJdUU130_provenance.
- NP435576.RAVfV2MRB8L6aKhISigIwhn9_G2XS6mxjxOHygIEhJdUU130_assertion evidence source_evidence_literature NP435576.RAVfV2MRB8L6aKhISigIwhn9_G2XS6mxjxOHygIEhJdUU130_provenance.
- NP435576.RAVfV2MRB8L6aKhISigIwhn9_G2XS6mxjxOHygIEhJdUU130_assertion description "[Mutations in SOX10 are associated with several neurocristopathies such as Waardenburg syndrome type IV (WS4), a congenital disorder characterized by the association of hearing loss, pigmentary abnormalities, and absence of ganglion cells in the myenteric and submucosal plexus of the gastrointestinal tract, also known as aganglionic megacolon or Hirschsprung disease (HSCR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435576.RAVfV2MRB8L6aKhISigIwhn9_G2XS6mxjxOHygIEhJdUU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP435576.RAVfV2MRB8L6aKhISigIwhn9_G2XS6mxjxOHygIEhJdUU130_provenance.