Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP627792.RA1Sh2oo1iMdJa1o7H3Ao_0TZr-utvnyDVI3iZN6pH47w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP627792.RA1Sh2oo1iMdJa1o7H3Ao_0TZr-utvnyDVI3iZN6pH47w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP627792.RA1Sh2oo1iMdJa1o7H3Ao_0TZr-utvnyDVI3iZN6pH47w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP627792.RA1Sh2oo1iMdJa1o7H3Ao_0TZr-utvnyDVI3iZN6pH47w130_provenance.
- NP627792.RA1Sh2oo1iMdJa1o7H3Ao_0TZr-utvnyDVI3iZN6pH47w130_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." NP627792.RA1Sh2oo1iMdJa1o7H3Ao_0TZr-utvnyDVI3iZN6pH47w130_provenance.
- NP627792.RA1Sh2oo1iMdJa1o7H3Ao_0TZr-utvnyDVI3iZN6pH47w130_assertion evidence source_evidence_literature NP627792.RA1Sh2oo1iMdJa1o7H3Ao_0TZr-utvnyDVI3iZN6pH47w130_provenance.
- NP627792.RA1Sh2oo1iMdJa1o7H3Ao_0TZr-utvnyDVI3iZN6pH47w130_assertion SIO_000772 23182313 NP627792.RA1Sh2oo1iMdJa1o7H3Ao_0TZr-utvnyDVI3iZN6pH47w130_provenance.
- NP627792.RA1Sh2oo1iMdJa1o7H3Ao_0TZr-utvnyDVI3iZN6pH47w130_assertion wasDerivedFrom befree-20150227 NP627792.RA1Sh2oo1iMdJa1o7H3Ao_0TZr-utvnyDVI3iZN6pH47w130_provenance.
- NP627792.RA1Sh2oo1iMdJa1o7H3Ao_0TZr-utvnyDVI3iZN6pH47w130_assertion wasGeneratedBy ECO_0000203 NP627792.RA1Sh2oo1iMdJa1o7H3Ao_0TZr-utvnyDVI3iZN6pH47w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP627792.RA1Sh2oo1iMdJa1o7H3Ao_0TZr-utvnyDVI3iZN6pH47w130_provenance.