Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_provenance.
- NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_assertion description "[Large deletions in Xq21 often are associated with contiguous gene syndromes consisting of X-linked deafness type 3 (DFN3), mental retardation (MRX), and choroideremia (CHM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_provenance.
- NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_assertion evidence source_evidence_literature NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_provenance.
- NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_assertion SIO_000772 10644430 NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_provenance.
- NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_assertion wasDerivedFrom befree-20140225 NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_provenance.
- NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_assertion wasGeneratedBy ECO_0000203 NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP208952.RADvfoJWK183EHNz3Y_vmAyUBmGLmZbd-7niia7TFIYFg130_provenance.