Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP734292.RA3WhcJC1KipHQYmR02FX1d-cKUlmaEK6fOltlnJda7ts130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP734292.RA3WhcJC1KipHQYmR02FX1d-cKUlmaEK6fOltlnJda7ts130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP734292.RA3WhcJC1KipHQYmR02FX1d-cKUlmaEK6fOltlnJda7ts130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP734292.RA3WhcJC1KipHQYmR02FX1d-cKUlmaEK6fOltlnJda7ts130_provenance.
- NP734292.RA3WhcJC1KipHQYmR02FX1d-cKUlmaEK6fOltlnJda7ts130_assertion wasGeneratedBy ECO_0000203 NP734292.RA3WhcJC1KipHQYmR02FX1d-cKUlmaEK6fOltlnJda7ts130_provenance.
- NP734292.RA3WhcJC1KipHQYmR02FX1d-cKUlmaEK6fOltlnJda7ts130_assertion wasDerivedFrom befree-20140225 NP734292.RA3WhcJC1KipHQYmR02FX1d-cKUlmaEK6fOltlnJda7ts130_provenance.
- NP734292.RA3WhcJC1KipHQYmR02FX1d-cKUlmaEK6fOltlnJda7ts130_assertion SIO_000772 1979048 NP734292.RA3WhcJC1KipHQYmR02FX1d-cKUlmaEK6fOltlnJda7ts130_provenance.
- NP734292.RA3WhcJC1KipHQYmR02FX1d-cKUlmaEK6fOltlnJda7ts130_assertion evidence source_evidence_literature NP734292.RA3WhcJC1KipHQYmR02FX1d-cKUlmaEK6fOltlnJda7ts130_provenance.
- NP734292.RA3WhcJC1KipHQYmR02FX1d-cKUlmaEK6fOltlnJda7ts130_assertion description "[Two independent familial STS deletions, one of which is associated with a phenotype of ichthyosis plus ocular albinism (XI/OA1) and the other with nystagmus plus Rud syndrome, lack some but not all of the normal S232 PFGE fragments.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734292.RA3WhcJC1KipHQYmR02FX1d-cKUlmaEK6fOltlnJda7ts130_provenance.
- befree-20140225 importedOn "2014-02-25" NP734292.RA3WhcJC1KipHQYmR02FX1d-cKUlmaEK6fOltlnJda7ts130_provenance.