Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP863504.RAudi_tuUGiLsroQ3b3Wp6LBr_155mk9qwW4FbJtHQ25Y130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP863504.RAudi_tuUGiLsroQ3b3Wp6LBr_155mk9qwW4FbJtHQ25Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP863504.RAudi_tuUGiLsroQ3b3Wp6LBr_155mk9qwW4FbJtHQ25Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP863504.RAudi_tuUGiLsroQ3b3Wp6LBr_155mk9qwW4FbJtHQ25Y130_provenance.
- NP863504.RAudi_tuUGiLsroQ3b3Wp6LBr_155mk9qwW4FbJtHQ25Y130_assertion description "[Mutations in the phospholipase A2 Group 6 (PLA2G6) gene have been identified in autosomal recessive neurodegenerative diseases classified as infantile neuroaxonal dystrophy and neurodegeneration with brain iron accumulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP863504.RAudi_tuUGiLsroQ3b3Wp6LBr_155mk9qwW4FbJtHQ25Y130_provenance.
- NP863504.RAudi_tuUGiLsroQ3b3Wp6LBr_155mk9qwW4FbJtHQ25Y130_assertion evidence source_evidence_literature NP863504.RAudi_tuUGiLsroQ3b3Wp6LBr_155mk9qwW4FbJtHQ25Y130_provenance.
- NP863504.RAudi_tuUGiLsroQ3b3Wp6LBr_155mk9qwW4FbJtHQ25Y130_assertion SIO_000772 23182313 NP863504.RAudi_tuUGiLsroQ3b3Wp6LBr_155mk9qwW4FbJtHQ25Y130_provenance.
- NP863504.RAudi_tuUGiLsroQ3b3Wp6LBr_155mk9qwW4FbJtHQ25Y130_assertion wasDerivedFrom befree-20140225 NP863504.RAudi_tuUGiLsroQ3b3Wp6LBr_155mk9qwW4FbJtHQ25Y130_provenance.
- NP863504.RAudi_tuUGiLsroQ3b3Wp6LBr_155mk9qwW4FbJtHQ25Y130_assertion wasGeneratedBy ECO_0000203 NP863504.RAudi_tuUGiLsroQ3b3Wp6LBr_155mk9qwW4FbJtHQ25Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP863504.RAudi_tuUGiLsroQ3b3Wp6LBr_155mk9qwW4FbJtHQ25Y130_provenance.