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- NP884595.RAqMtDnIVx1h2jBe2JqhmzLjlYjz7DBkM1-yUB6kdKBRc130_assertion type Assertion NP884595.RAqMtDnIVx1h2jBe2JqhmzLjlYjz7DBkM1-yUB6kdKBRc130_head.
- NP884595.RAqMtDnIVx1h2jBe2JqhmzLjlYjz7DBkM1-yUB6kdKBRc130_assertion description "[Ataxia with oculomotor apraxia type1 (AOA1): novel and recurrent aprataxin mutations, coenzyme Q10 analyses, and clinical findings in Italian patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP884595.RAqMtDnIVx1h2jBe2JqhmzLjlYjz7DBkM1-yUB6kdKBRc130_provenance.
- NP884595.RAqMtDnIVx1h2jBe2JqhmzLjlYjz7DBkM1-yUB6kdKBRc130_assertion evidence source_evidence_literature NP884595.RAqMtDnIVx1h2jBe2JqhmzLjlYjz7DBkM1-yUB6kdKBRc130_provenance.
- NP884595.RAqMtDnIVx1h2jBe2JqhmzLjlYjz7DBkM1-yUB6kdKBRc130_assertion SIO_000772 21465257 NP884595.RAqMtDnIVx1h2jBe2JqhmzLjlYjz7DBkM1-yUB6kdKBRc130_provenance.
- NP884595.RAqMtDnIVx1h2jBe2JqhmzLjlYjz7DBkM1-yUB6kdKBRc130_assertion wasDerivedFrom befree-2016 NP884595.RAqMtDnIVx1h2jBe2JqhmzLjlYjz7DBkM1-yUB6kdKBRc130_provenance.
- NP884595.RAqMtDnIVx1h2jBe2JqhmzLjlYjz7DBkM1-yUB6kdKBRc130_assertion wasGeneratedBy ECO_0000203 NP884595.RAqMtDnIVx1h2jBe2JqhmzLjlYjz7DBkM1-yUB6kdKBRc130_provenance.