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- source_evidence_literature type ECO_0000212 NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_provenance.
- NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_assertion description "[Overrepresentation of the founder PPOX gene mutation R59W in a South African patient with severe clinical manifestation of porphyria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_provenance.
- NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_assertion evidence source_evidence_literature NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_provenance.
- NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_assertion SIO_000772 15660919 NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_provenance.
- NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_assertion wasDerivedFrom befree-20150227 NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_provenance.
- NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_assertion wasGeneratedBy ECO_0000203 NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_provenance.
- befree-20150227 importedOn "2015-02-27" NP638489.RA7u6U8911GaRygtCNcFSpmzJPGtF06JohK5MY8M_Bsew130_provenance.