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- source_evidence_literature type ECO_0000212 NP463965.RAQTGCjsS7SlXigoN0Vf2BIQTR-vmAhfb6-pCXOWAK7fM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP463965.RAQTGCjsS7SlXigoN0Vf2BIQTR-vmAhfb6-pCXOWAK7fM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP463965.RAQTGCjsS7SlXigoN0Vf2BIQTR-vmAhfb6-pCXOWAK7fM130_provenance.
- NP463965.RAQTGCjsS7SlXigoN0Vf2BIQTR-vmAhfb6-pCXOWAK7fM130_assertion description "[Methemoglobinemia, the first hereditary disease to be identified that involved an enzyme deficiency, has been ascribed to mutations in the enzyme cytochrome b(5) reductase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463965.RAQTGCjsS7SlXigoN0Vf2BIQTR-vmAhfb6-pCXOWAK7fM130_provenance.
- NP463965.RAQTGCjsS7SlXigoN0Vf2BIQTR-vmAhfb6-pCXOWAK7fM130_assertion evidence source_evidence_literature NP463965.RAQTGCjsS7SlXigoN0Vf2BIQTR-vmAhfb6-pCXOWAK7fM130_provenance.
- NP463965.RAQTGCjsS7SlXigoN0Vf2BIQTR-vmAhfb6-pCXOWAK7fM130_assertion SIO_000772 14609324 NP463965.RAQTGCjsS7SlXigoN0Vf2BIQTR-vmAhfb6-pCXOWAK7fM130_provenance.
- NP463965.RAQTGCjsS7SlXigoN0Vf2BIQTR-vmAhfb6-pCXOWAK7fM130_assertion wasDerivedFrom befree-20140225 NP463965.RAQTGCjsS7SlXigoN0Vf2BIQTR-vmAhfb6-pCXOWAK7fM130_provenance.
- NP463965.RAQTGCjsS7SlXigoN0Vf2BIQTR-vmAhfb6-pCXOWAK7fM130_assertion wasGeneratedBy ECO_0000203 NP463965.RAQTGCjsS7SlXigoN0Vf2BIQTR-vmAhfb6-pCXOWAK7fM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP463965.RAQTGCjsS7SlXigoN0Vf2BIQTR-vmAhfb6-pCXOWAK7fM130_provenance.