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- NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_assertion type Assertion NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_head.
- NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_assertion description "[The molecular genetic analysis demonstrated the APTX mutation W279X at locus 9p13.3 (ataxia with oculomotor apraxia 1 disease), and psychologic studies showed mild cognitive impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_provenance.
- NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_assertion evidence source_evidence_literature NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_provenance.
- NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_assertion SIO_000772 15996403 NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_provenance.
- NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_assertion wasDerivedFrom befree-2016 NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_provenance.
- NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_assertion wasGeneratedBy ECO_0000203 NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_provenance.