Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP727034.RAl3CK6mdFAqpqCo2sTQSuwVUPjMyc3Pf0dWBZE0bNJyE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP727034.RAl3CK6mdFAqpqCo2sTQSuwVUPjMyc3Pf0dWBZE0bNJyE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP727034.RAl3CK6mdFAqpqCo2sTQSuwVUPjMyc3Pf0dWBZE0bNJyE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP727034.RAl3CK6mdFAqpqCo2sTQSuwVUPjMyc3Pf0dWBZE0bNJyE130_provenance.
- NP727034.RAl3CK6mdFAqpqCo2sTQSuwVUPjMyc3Pf0dWBZE0bNJyE130_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." NP727034.RAl3CK6mdFAqpqCo2sTQSuwVUPjMyc3Pf0dWBZE0bNJyE130_provenance.
- NP727034.RAl3CK6mdFAqpqCo2sTQSuwVUPjMyc3Pf0dWBZE0bNJyE130_assertion evidence source_evidence_literature NP727034.RAl3CK6mdFAqpqCo2sTQSuwVUPjMyc3Pf0dWBZE0bNJyE130_provenance.
- NP727034.RAl3CK6mdFAqpqCo2sTQSuwVUPjMyc3Pf0dWBZE0bNJyE130_assertion SIO_000772 23182313 NP727034.RAl3CK6mdFAqpqCo2sTQSuwVUPjMyc3Pf0dWBZE0bNJyE130_provenance.
- NP727034.RAl3CK6mdFAqpqCo2sTQSuwVUPjMyc3Pf0dWBZE0bNJyE130_assertion wasDerivedFrom befree-20140225 NP727034.RAl3CK6mdFAqpqCo2sTQSuwVUPjMyc3Pf0dWBZE0bNJyE130_provenance.
- NP727034.RAl3CK6mdFAqpqCo2sTQSuwVUPjMyc3Pf0dWBZE0bNJyE130_assertion wasGeneratedBy ECO_0000203 NP727034.RAl3CK6mdFAqpqCo2sTQSuwVUPjMyc3Pf0dWBZE0bNJyE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP727034.RAl3CK6mdFAqpqCo2sTQSuwVUPjMyc3Pf0dWBZE0bNJyE130_provenance.