Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP276268.RAKAeYM1CscvMq49Vx_CYgwMD16_4Kmw7yCBB5cU_v4v8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP276268.RAKAeYM1CscvMq49Vx_CYgwMD16_4Kmw7yCBB5cU_v4v8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP276268.RAKAeYM1CscvMq49Vx_CYgwMD16_4Kmw7yCBB5cU_v4v8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP276268.RAKAeYM1CscvMq49Vx_CYgwMD16_4Kmw7yCBB5cU_v4v8130_provenance.
- NP276268.RAKAeYM1CscvMq49Vx_CYgwMD16_4Kmw7yCBB5cU_v4v8130_assertion description "[These observations suggest that inactivating defects within the VDR gene do not commonly contribute to the primary pathogenesis of severe refractory hyperparathyroidism in uremia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP276268.RAKAeYM1CscvMq49Vx_CYgwMD16_4Kmw7yCBB5cU_v4v8130_provenance.
- NP276268.RAKAeYM1CscvMq49Vx_CYgwMD16_4Kmw7yCBB5cU_v4v8130_assertion evidence source_evidence_literature NP276268.RAKAeYM1CscvMq49Vx_CYgwMD16_4Kmw7yCBB5cU_v4v8130_provenance.
- NP276268.RAKAeYM1CscvMq49Vx_CYgwMD16_4Kmw7yCBB5cU_v4v8130_assertion SIO_000772 10690903 NP276268.RAKAeYM1CscvMq49Vx_CYgwMD16_4Kmw7yCBB5cU_v4v8130_provenance.
- NP276268.RAKAeYM1CscvMq49Vx_CYgwMD16_4Kmw7yCBB5cU_v4v8130_assertion wasDerivedFrom befree-2016 NP276268.RAKAeYM1CscvMq49Vx_CYgwMD16_4Kmw7yCBB5cU_v4v8130_provenance.
- NP276268.RAKAeYM1CscvMq49Vx_CYgwMD16_4Kmw7yCBB5cU_v4v8130_assertion wasGeneratedBy ECO_0000203 NP276268.RAKAeYM1CscvMq49Vx_CYgwMD16_4Kmw7yCBB5cU_v4v8130_provenance.
- befree-2016 importedOn "2016-02-19" NP276268.RAKAeYM1CscvMq49Vx_CYgwMD16_4Kmw7yCBB5cU_v4v8130_provenance.