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- source_evidence_literature type ECO_0000212 NP97799.RArqmKBrXhPV7EnQNdpaFKwHYVr48kXr2PlaBWUKL-cgw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP97799.RArqmKBrXhPV7EnQNdpaFKwHYVr48kXr2PlaBWUKL-cgw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP97799.RArqmKBrXhPV7EnQNdpaFKwHYVr48kXr2PlaBWUKL-cgw130_provenance.
- NP97799.RArqmKBrXhPV7EnQNdpaFKwHYVr48kXr2PlaBWUKL-cgw130_assertion description "[Mutations in the haemoglobin beta-globin (HbB) and glucose-6-phosphate dehydrogenase (G6PD) genes cause widespread human genetic disorders such as sickle cell diseases and G6PD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP97799.RArqmKBrXhPV7EnQNdpaFKwHYVr48kXr2PlaBWUKL-cgw130_provenance.
- NP97799.RArqmKBrXhPV7EnQNdpaFKwHYVr48kXr2PlaBWUKL-cgw130_assertion evidence source_evidence_literature NP97799.RArqmKBrXhPV7EnQNdpaFKwHYVr48kXr2PlaBWUKL-cgw130_provenance.
- NP97799.RArqmKBrXhPV7EnQNdpaFKwHYVr48kXr2PlaBWUKL-cgw130_assertion SIO_000772 16356170 NP97799.RArqmKBrXhPV7EnQNdpaFKwHYVr48kXr2PlaBWUKL-cgw130_provenance.
- NP97799.RArqmKBrXhPV7EnQNdpaFKwHYVr48kXr2PlaBWUKL-cgw130_assertion wasDerivedFrom gad-20150221 NP97799.RArqmKBrXhPV7EnQNdpaFKwHYVr48kXr2PlaBWUKL-cgw130_provenance.
- NP97799.RArqmKBrXhPV7EnQNdpaFKwHYVr48kXr2PlaBWUKL-cgw130_assertion wasGeneratedBy ECO_0000203 NP97799.RArqmKBrXhPV7EnQNdpaFKwHYVr48kXr2PlaBWUKL-cgw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP97799.RArqmKBrXhPV7EnQNdpaFKwHYVr48kXr2PlaBWUKL-cgw130_provenance.