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- source_evidence_literature type ECO_0000212 NP254964.RAaZwatgfOQWs83Ec6uu5V2mBr-ItNa7_UxcBhfQ35Sug130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP254964.RAaZwatgfOQWs83Ec6uu5V2mBr-ItNa7_UxcBhfQ35Sug130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP254964.RAaZwatgfOQWs83Ec6uu5V2mBr-ItNa7_UxcBhfQ35Sug130_provenance.
- NP254964.RAaZwatgfOQWs83Ec6uu5V2mBr-ItNa7_UxcBhfQ35Sug130_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." NP254964.RAaZwatgfOQWs83Ec6uu5V2mBr-ItNa7_UxcBhfQ35Sug130_provenance.
- NP254964.RAaZwatgfOQWs83Ec6uu5V2mBr-ItNa7_UxcBhfQ35Sug130_assertion evidence source_evidence_literature NP254964.RAaZwatgfOQWs83Ec6uu5V2mBr-ItNa7_UxcBhfQ35Sug130_provenance.
- NP254964.RAaZwatgfOQWs83Ec6uu5V2mBr-ItNa7_UxcBhfQ35Sug130_assertion SIO_000772 23941260 NP254964.RAaZwatgfOQWs83Ec6uu5V2mBr-ItNa7_UxcBhfQ35Sug130_provenance.
- NP254964.RAaZwatgfOQWs83Ec6uu5V2mBr-ItNa7_UxcBhfQ35Sug130_assertion wasDerivedFrom befree-20150227 NP254964.RAaZwatgfOQWs83Ec6uu5V2mBr-ItNa7_UxcBhfQ35Sug130_provenance.
- NP254964.RAaZwatgfOQWs83Ec6uu5V2mBr-ItNa7_UxcBhfQ35Sug130_assertion wasGeneratedBy ECO_0000203 NP254964.RAaZwatgfOQWs83Ec6uu5V2mBr-ItNa7_UxcBhfQ35Sug130_provenance.
- befree-20150227 importedOn "2015-02-27" NP254964.RAaZwatgfOQWs83Ec6uu5V2mBr-ItNa7_UxcBhfQ35Sug130_provenance.