Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1031206.RAhiuOQEenYW22xch0qeeUyBUO38i9nAkJYPsPkQtR4vw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1031206.RAhiuOQEenYW22xch0qeeUyBUO38i9nAkJYPsPkQtR4vw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1031206.RAhiuOQEenYW22xch0qeeUyBUO38i9nAkJYPsPkQtR4vw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1031206.RAhiuOQEenYW22xch0qeeUyBUO38i9nAkJYPsPkQtR4vw130_provenance.
- NP1031206.RAhiuOQEenYW22xch0qeeUyBUO38i9nAkJYPsPkQtR4vw130_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." NP1031206.RAhiuOQEenYW22xch0qeeUyBUO38i9nAkJYPsPkQtR4vw130_provenance.
- NP1031206.RAhiuOQEenYW22xch0qeeUyBUO38i9nAkJYPsPkQtR4vw130_assertion evidence source_evidence_literature NP1031206.RAhiuOQEenYW22xch0qeeUyBUO38i9nAkJYPsPkQtR4vw130_provenance.
- NP1031206.RAhiuOQEenYW22xch0qeeUyBUO38i9nAkJYPsPkQtR4vw130_assertion SIO_000772 23182313 NP1031206.RAhiuOQEenYW22xch0qeeUyBUO38i9nAkJYPsPkQtR4vw130_provenance.
- NP1031206.RAhiuOQEenYW22xch0qeeUyBUO38i9nAkJYPsPkQtR4vw130_assertion wasDerivedFrom befree-2016 NP1031206.RAhiuOQEenYW22xch0qeeUyBUO38i9nAkJYPsPkQtR4vw130_provenance.
- NP1031206.RAhiuOQEenYW22xch0qeeUyBUO38i9nAkJYPsPkQtR4vw130_assertion wasGeneratedBy ECO_0000203 NP1031206.RAhiuOQEenYW22xch0qeeUyBUO38i9nAkJYPsPkQtR4vw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1031206.RAhiuOQEenYW22xch0qeeUyBUO38i9nAkJYPsPkQtR4vw130_provenance.