Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP197064.RArvPa_Z0nQGWTbssVN0HkJcDm0wdRWfLoPeKAFpp1Xlc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP197064.RArvPa_Z0nQGWTbssVN0HkJcDm0wdRWfLoPeKAFpp1Xlc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP197064.RArvPa_Z0nQGWTbssVN0HkJcDm0wdRWfLoPeKAFpp1Xlc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP197064.RArvPa_Z0nQGWTbssVN0HkJcDm0wdRWfLoPeKAFpp1Xlc130_provenance.
- NP197064.RArvPa_Z0nQGWTbssVN0HkJcDm0wdRWfLoPeKAFpp1Xlc130_assertion description "[Mutations in SCO2, a cytochrome c oxidase (COX) assembly gene located on chromosome 22, have recently been reported in patients with fatal infantile cardio-encephalomyopathy and severe COX deficiency in heart and skeletal muscle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP197064.RArvPa_Z0nQGWTbssVN0HkJcDm0wdRWfLoPeKAFpp1Xlc130_provenance.
- NP197064.RArvPa_Z0nQGWTbssVN0HkJcDm0wdRWfLoPeKAFpp1Xlc130_assertion evidence source_evidence_literature NP197064.RArvPa_Z0nQGWTbssVN0HkJcDm0wdRWfLoPeKAFpp1Xlc130_provenance.
- NP197064.RArvPa_Z0nQGWTbssVN0HkJcDm0wdRWfLoPeKAFpp1Xlc130_assertion SIO_000772 10749987 NP197064.RArvPa_Z0nQGWTbssVN0HkJcDm0wdRWfLoPeKAFpp1Xlc130_provenance.
- NP197064.RArvPa_Z0nQGWTbssVN0HkJcDm0wdRWfLoPeKAFpp1Xlc130_assertion wasDerivedFrom befree-20140225 NP197064.RArvPa_Z0nQGWTbssVN0HkJcDm0wdRWfLoPeKAFpp1Xlc130_provenance.
- NP197064.RArvPa_Z0nQGWTbssVN0HkJcDm0wdRWfLoPeKAFpp1Xlc130_assertion wasGeneratedBy ECO_0000203 NP197064.RArvPa_Z0nQGWTbssVN0HkJcDm0wdRWfLoPeKAFpp1Xlc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP197064.RArvPa_Z0nQGWTbssVN0HkJcDm0wdRWfLoPeKAFpp1Xlc130_provenance.