Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP761491.RAVSla8aOP2c7nZ9NMJdrw3nbPPOXMkCL5F1IgLiBpBOQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP761491.RAVSla8aOP2c7nZ9NMJdrw3nbPPOXMkCL5F1IgLiBpBOQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP761491.RAVSla8aOP2c7nZ9NMJdrw3nbPPOXMkCL5F1IgLiBpBOQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP761491.RAVSla8aOP2c7nZ9NMJdrw3nbPPOXMkCL5F1IgLiBpBOQ130_provenance.
- NP761491.RAVSla8aOP2c7nZ9NMJdrw3nbPPOXMkCL5F1IgLiBpBOQ130_assertion description "[Heritable mutations in the ttpA gene, encoding for TTP, result in ataxia with vitamin E deficiency (AVED) syndrome, typified by low vitamin E levels and a plethora of neurological disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761491.RAVSla8aOP2c7nZ9NMJdrw3nbPPOXMkCL5F1IgLiBpBOQ130_provenance.
- NP761491.RAVSla8aOP2c7nZ9NMJdrw3nbPPOXMkCL5F1IgLiBpBOQ130_assertion evidence source_evidence_literature NP761491.RAVSla8aOP2c7nZ9NMJdrw3nbPPOXMkCL5F1IgLiBpBOQ130_provenance.
- NP761491.RAVSla8aOP2c7nZ9NMJdrw3nbPPOXMkCL5F1IgLiBpBOQ130_assertion SIO_000772 16819822 NP761491.RAVSla8aOP2c7nZ9NMJdrw3nbPPOXMkCL5F1IgLiBpBOQ130_provenance.
- NP761491.RAVSla8aOP2c7nZ9NMJdrw3nbPPOXMkCL5F1IgLiBpBOQ130_assertion wasDerivedFrom befree-20150227 NP761491.RAVSla8aOP2c7nZ9NMJdrw3nbPPOXMkCL5F1IgLiBpBOQ130_provenance.
- NP761491.RAVSla8aOP2c7nZ9NMJdrw3nbPPOXMkCL5F1IgLiBpBOQ130_assertion wasGeneratedBy ECO_0000203 NP761491.RAVSla8aOP2c7nZ9NMJdrw3nbPPOXMkCL5F1IgLiBpBOQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP761491.RAVSla8aOP2c7nZ9NMJdrw3nbPPOXMkCL5F1IgLiBpBOQ130_provenance.