Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7626.RAQFUM3HNEQAr0VmO5G2F6c6tSGI2qCwbljy_HV29pVyQ130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7626.RAQFUM3HNEQAr0VmO5G2F6c6tSGI2qCwbljy_HV29pVyQ130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7626.RAQFUM3HNEQAr0VmO5G2F6c6tSGI2qCwbljy_HV29pVyQ130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7626.RAQFUM3HNEQAr0VmO5G2F6c6tSGI2qCwbljy_HV29pVyQ130_provenance.
- NP7626.RAQFUM3HNEQAr0VmO5G2F6c6tSGI2qCwbljy_HV29pVyQ130_assertion description "[Ataxia with oculomotor apraxia defines a group of genetically distinct recessive ataxias including ataxia-telangectasia (A-T, ATM gene), ataxia with oculomotor apraxia type 1 (AOA1, APTX gene) and type 2 (AOA2, SETX gene).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7626.RAQFUM3HNEQAr0VmO5G2F6c6tSGI2qCwbljy_HV29pVyQ130_provenance.
- NP7626.RAQFUM3HNEQAr0VmO5G2F6c6tSGI2qCwbljy_HV29pVyQ130_assertion evidence source_evidence_curated NP7626.RAQFUM3HNEQAr0VmO5G2F6c6tSGI2qCwbljy_HV29pVyQ130_provenance.
- NP7626.RAQFUM3HNEQAr0VmO5G2F6c6tSGI2qCwbljy_HV29pVyQ130_assertion SIO_000772 23941260 NP7626.RAQFUM3HNEQAr0VmO5G2F6c6tSGI2qCwbljy_HV29pVyQ130_provenance.
- NP7626.RAQFUM3HNEQAr0VmO5G2F6c6tSGI2qCwbljy_HV29pVyQ130_assertion wasDerivedFrom uniprot-2016 NP7626.RAQFUM3HNEQAr0VmO5G2F6c6tSGI2qCwbljy_HV29pVyQ130_provenance.
- NP7626.RAQFUM3HNEQAr0VmO5G2F6c6tSGI2qCwbljy_HV29pVyQ130_assertion wasGeneratedBy ECO_0000218 NP7626.RAQFUM3HNEQAr0VmO5G2F6c6tSGI2qCwbljy_HV29pVyQ130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP7626.RAQFUM3HNEQAr0VmO5G2F6c6tSGI2qCwbljy_HV29pVyQ130_provenance.