Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP687817.RAnZElnlqVbJkdihwnnIGvIAZBkY6Z9KJFtByDptRZciE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP687817.RAnZElnlqVbJkdihwnnIGvIAZBkY6Z9KJFtByDptRZciE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP687817.RAnZElnlqVbJkdihwnnIGvIAZBkY6Z9KJFtByDptRZciE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP687817.RAnZElnlqVbJkdihwnnIGvIAZBkY6Z9KJFtByDptRZciE130_provenance.
- NP687817.RAnZElnlqVbJkdihwnnIGvIAZBkY6Z9KJFtByDptRZciE130_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." NP687817.RAnZElnlqVbJkdihwnnIGvIAZBkY6Z9KJFtByDptRZciE130_provenance.
- NP687817.RAnZElnlqVbJkdihwnnIGvIAZBkY6Z9KJFtByDptRZciE130_assertion evidence source_evidence_literature NP687817.RAnZElnlqVbJkdihwnnIGvIAZBkY6Z9KJFtByDptRZciE130_provenance.
- NP687817.RAnZElnlqVbJkdihwnnIGvIAZBkY6Z9KJFtByDptRZciE130_assertion SIO_000772 10798354 NP687817.RAnZElnlqVbJkdihwnnIGvIAZBkY6Z9KJFtByDptRZciE130_provenance.
- NP687817.RAnZElnlqVbJkdihwnnIGvIAZBkY6Z9KJFtByDptRZciE130_assertion wasDerivedFrom befree-20140225 NP687817.RAnZElnlqVbJkdihwnnIGvIAZBkY6Z9KJFtByDptRZciE130_provenance.
- NP687817.RAnZElnlqVbJkdihwnnIGvIAZBkY6Z9KJFtByDptRZciE130_assertion wasGeneratedBy ECO_0000203 NP687817.RAnZElnlqVbJkdihwnnIGvIAZBkY6Z9KJFtByDptRZciE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP687817.RAnZElnlqVbJkdihwnnIGvIAZBkY6Z9KJFtByDptRZciE130_provenance.