Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_assertion> ?p ?o ?g. }
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- NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_assertion type Assertion NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_head.
- NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_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." NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_provenance.
- NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_assertion evidence source_evidence_literature NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_provenance.
- NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_assertion SIO_000772 21465257 NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_provenance.
- NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_assertion wasDerivedFrom befree-20150227 NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_provenance.
- NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_assertion wasGeneratedBy ECO_0000203 NP914818.RALHMLo9aMMABpUPQ3imE-Isj_bB7uzHtscdAmVzN1avE130_provenance.