Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP389751.RAl26bd49FcZ8J3LiwrrKqrrWXeiGCl3W5rHVVUguVmVQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP389751.RAl26bd49FcZ8J3LiwrrKqrrWXeiGCl3W5rHVVUguVmVQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP389751.RAl26bd49FcZ8J3LiwrrKqrrWXeiGCl3W5rHVVUguVmVQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP389751.RAl26bd49FcZ8J3LiwrrKqrrWXeiGCl3W5rHVVUguVmVQ130_provenance.
- NP389751.RAl26bd49FcZ8J3LiwrrKqrrWXeiGCl3W5rHVVUguVmVQ130_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." NP389751.RAl26bd49FcZ8J3LiwrrKqrrWXeiGCl3W5rHVVUguVmVQ130_provenance.
- NP389751.RAl26bd49FcZ8J3LiwrrKqrrWXeiGCl3W5rHVVUguVmVQ130_assertion evidence source_evidence_literature NP389751.RAl26bd49FcZ8J3LiwrrKqrrWXeiGCl3W5rHVVUguVmVQ130_provenance.
- NP389751.RAl26bd49FcZ8J3LiwrrKqrrWXeiGCl3W5rHVVUguVmVQ130_assertion SIO_000772 23182313 NP389751.RAl26bd49FcZ8J3LiwrrKqrrWXeiGCl3W5rHVVUguVmVQ130_provenance.
- NP389751.RAl26bd49FcZ8J3LiwrrKqrrWXeiGCl3W5rHVVUguVmVQ130_assertion wasDerivedFrom befree-20140225 NP389751.RAl26bd49FcZ8J3LiwrrKqrrWXeiGCl3W5rHVVUguVmVQ130_provenance.
- NP389751.RAl26bd49FcZ8J3LiwrrKqrrWXeiGCl3W5rHVVUguVmVQ130_assertion wasGeneratedBy ECO_0000203 NP389751.RAl26bd49FcZ8J3LiwrrKqrrWXeiGCl3W5rHVVUguVmVQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP389751.RAl26bd49FcZ8J3LiwrrKqrrWXeiGCl3W5rHVVUguVmVQ130_provenance.