Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP409221.RAx9pApE_ELqmHVTqpnR_nvIY97ThnqdyCdV5eLXg_F00130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP409221.RAx9pApE_ELqmHVTqpnR_nvIY97ThnqdyCdV5eLXg_F00130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP409221.RAx9pApE_ELqmHVTqpnR_nvIY97ThnqdyCdV5eLXg_F00130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP409221.RAx9pApE_ELqmHVTqpnR_nvIY97ThnqdyCdV5eLXg_F00130_provenance.
- NP409221.RAx9pApE_ELqmHVTqpnR_nvIY97ThnqdyCdV5eLXg_F00130_assertion description "[A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP409221.RAx9pApE_ELqmHVTqpnR_nvIY97ThnqdyCdV5eLXg_F00130_provenance.
- NP409221.RAx9pApE_ELqmHVTqpnR_nvIY97ThnqdyCdV5eLXg_F00130_assertion evidence source_evidence_literature NP409221.RAx9pApE_ELqmHVTqpnR_nvIY97ThnqdyCdV5eLXg_F00130_provenance.
- NP409221.RAx9pApE_ELqmHVTqpnR_nvIY97ThnqdyCdV5eLXg_F00130_assertion SIO_000772 11326269 NP409221.RAx9pApE_ELqmHVTqpnR_nvIY97ThnqdyCdV5eLXg_F00130_provenance.
- NP409221.RAx9pApE_ELqmHVTqpnR_nvIY97ThnqdyCdV5eLXg_F00130_assertion wasDerivedFrom befree-20140225 NP409221.RAx9pApE_ELqmHVTqpnR_nvIY97ThnqdyCdV5eLXg_F00130_provenance.
- NP409221.RAx9pApE_ELqmHVTqpnR_nvIY97ThnqdyCdV5eLXg_F00130_assertion wasGeneratedBy ECO_0000203 NP409221.RAx9pApE_ELqmHVTqpnR_nvIY97ThnqdyCdV5eLXg_F00130_provenance.
- befree-20140225 importedOn "2014-02-25" NP409221.RAx9pApE_ELqmHVTqpnR_nvIY97ThnqdyCdV5eLXg_F00130_provenance.