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- source_evidence_literature type ECO_0000212 NP825929.RA7WApHBNKLJfSdL3y9gmIdge9ZJ4bHxttC7Ex3hMpMWY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP825929.RA7WApHBNKLJfSdL3y9gmIdge9ZJ4bHxttC7Ex3hMpMWY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP825929.RA7WApHBNKLJfSdL3y9gmIdge9ZJ4bHxttC7Ex3hMpMWY130_provenance.
- NP825929.RA7WApHBNKLJfSdL3y9gmIdge9ZJ4bHxttC7Ex3hMpMWY130_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." NP825929.RA7WApHBNKLJfSdL3y9gmIdge9ZJ4bHxttC7Ex3hMpMWY130_provenance.
- NP825929.RA7WApHBNKLJfSdL3y9gmIdge9ZJ4bHxttC7Ex3hMpMWY130_assertion evidence source_evidence_literature NP825929.RA7WApHBNKLJfSdL3y9gmIdge9ZJ4bHxttC7Ex3hMpMWY130_provenance.
- NP825929.RA7WApHBNKLJfSdL3y9gmIdge9ZJ4bHxttC7Ex3hMpMWY130_assertion SIO_000772 20629144 NP825929.RA7WApHBNKLJfSdL3y9gmIdge9ZJ4bHxttC7Ex3hMpMWY130_provenance.
- NP825929.RA7WApHBNKLJfSdL3y9gmIdge9ZJ4bHxttC7Ex3hMpMWY130_assertion wasDerivedFrom befree-2016 NP825929.RA7WApHBNKLJfSdL3y9gmIdge9ZJ4bHxttC7Ex3hMpMWY130_provenance.
- NP825929.RA7WApHBNKLJfSdL3y9gmIdge9ZJ4bHxttC7Ex3hMpMWY130_assertion wasGeneratedBy ECO_0000203 NP825929.RA7WApHBNKLJfSdL3y9gmIdge9ZJ4bHxttC7Ex3hMpMWY130_provenance.
- befree-2016 importedOn "2016-02-19" NP825929.RA7WApHBNKLJfSdL3y9gmIdge9ZJ4bHxttC7Ex3hMpMWY130_provenance.