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- NP388836.RAAntTICmqHiu6HXU_x1sDcITwHEr86ZiLbVjw8Ihalr0130_assertion type Assertion NP388836.RAAntTICmqHiu6HXU_x1sDcITwHEr86ZiLbVjw8Ihalr0130_head.
- NP388836.RAAntTICmqHiu6HXU_x1sDcITwHEr86ZiLbVjw8Ihalr0130_assertion wasGeneratedBy ECO_0000203 NP388836.RAAntTICmqHiu6HXU_x1sDcITwHEr86ZiLbVjw8Ihalr0130_provenance.
- NP388836.RAAntTICmqHiu6HXU_x1sDcITwHEr86ZiLbVjw8Ihalr0130_assertion wasDerivedFrom befree-20140225 NP388836.RAAntTICmqHiu6HXU_x1sDcITwHEr86ZiLbVjw8Ihalr0130_provenance.
- NP388836.RAAntTICmqHiu6HXU_x1sDcITwHEr86ZiLbVjw8Ihalr0130_assertion SIO_000772 21844581 NP388836.RAAntTICmqHiu6HXU_x1sDcITwHEr86ZiLbVjw8Ihalr0130_provenance.
- NP388836.RAAntTICmqHiu6HXU_x1sDcITwHEr86ZiLbVjw8Ihalr0130_assertion evidence source_evidence_literature NP388836.RAAntTICmqHiu6HXU_x1sDcITwHEr86ZiLbVjw8Ihalr0130_provenance.
- NP388836.RAAntTICmqHiu6HXU_x1sDcITwHEr86ZiLbVjw8Ihalr0130_assertion description "[A novel PHKA2 gross deletion mutation in a Korean patient with X-linked liver glycogenosis type I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP388836.RAAntTICmqHiu6HXU_x1sDcITwHEr86ZiLbVjw8Ihalr0130_provenance.