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- source_evidence_literature type ECO_0000212 NP795475.RABm7IERkIUbAodsqhpMBKzzvkH3s2HQDBMfA3cLYsqpI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP795475.RABm7IERkIUbAodsqhpMBKzzvkH3s2HQDBMfA3cLYsqpI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP795475.RABm7IERkIUbAodsqhpMBKzzvkH3s2HQDBMfA3cLYsqpI130_provenance.
- NP795475.RABm7IERkIUbAodsqhpMBKzzvkH3s2HQDBMfA3cLYsqpI130_assertion description "[All patients were screened for abnormalities in serum ceruloplasmin and ferritin levels and mutations in NBIA-associated genes [pantothenate kinase 2 (PANK2), PLA2G6 and ferritin light chain (exon 4)].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP795475.RABm7IERkIUbAodsqhpMBKzzvkH3s2HQDBMfA3cLYsqpI130_provenance.
- NP795475.RABm7IERkIUbAodsqhpMBKzzvkH3s2HQDBMfA3cLYsqpI130_assertion evidence source_evidence_literature NP795475.RABm7IERkIUbAodsqhpMBKzzvkH3s2HQDBMfA3cLYsqpI130_provenance.
- NP795475.RABm7IERkIUbAodsqhpMBKzzvkH3s2HQDBMfA3cLYsqpI130_assertion SIO_000772 20629144 NP795475.RABm7IERkIUbAodsqhpMBKzzvkH3s2HQDBMfA3cLYsqpI130_provenance.
- NP795475.RABm7IERkIUbAodsqhpMBKzzvkH3s2HQDBMfA3cLYsqpI130_assertion wasDerivedFrom befree-20150227 NP795475.RABm7IERkIUbAodsqhpMBKzzvkH3s2HQDBMfA3cLYsqpI130_provenance.
- NP795475.RABm7IERkIUbAodsqhpMBKzzvkH3s2HQDBMfA3cLYsqpI130_assertion wasGeneratedBy ECO_0000203 NP795475.RABm7IERkIUbAodsqhpMBKzzvkH3s2HQDBMfA3cLYsqpI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP795475.RABm7IERkIUbAodsqhpMBKzzvkH3s2HQDBMfA3cLYsqpI130_provenance.