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- source_evidence_literature type ECO_0000212 NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_provenance.
- NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_assertion wasGeneratedBy ECO_0000203 NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_provenance.
- NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_assertion wasDerivedFrom befree-20140225 NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_provenance.
- NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_assertion SIO_000772 1979048 NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_provenance.
- NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_assertion evidence source_evidence_literature NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_provenance.
- NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_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." NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP563502.RAvSbdbKTTQ5VcyOpNEOmUtOA9gyFLWMs2AtrE_7TzwzM130_provenance.