Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP792205.RAG7PaNm28L5983xRxZQTWve5-NN2SyuNeMbdleub1cP4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP792205.RAG7PaNm28L5983xRxZQTWve5-NN2SyuNeMbdleub1cP4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP792205.RAG7PaNm28L5983xRxZQTWve5-NN2SyuNeMbdleub1cP4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP792205.RAG7PaNm28L5983xRxZQTWve5-NN2SyuNeMbdleub1cP4130_provenance.
- NP792205.RAG7PaNm28L5983xRxZQTWve5-NN2SyuNeMbdleub1cP4130_assertion description "[In white individuals, the A1166C 3'-UTR variant of angiotensin II type 1 receptor (AT1R) has been associated with CKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP792205.RAG7PaNm28L5983xRxZQTWve5-NN2SyuNeMbdleub1cP4130_provenance.
- NP792205.RAG7PaNm28L5983xRxZQTWve5-NN2SyuNeMbdleub1cP4130_assertion evidence source_evidence_literature NP792205.RAG7PaNm28L5983xRxZQTWve5-NN2SyuNeMbdleub1cP4130_provenance.
- NP792205.RAG7PaNm28L5983xRxZQTWve5-NN2SyuNeMbdleub1cP4130_assertion SIO_000772 16396964 NP792205.RAG7PaNm28L5983xRxZQTWve5-NN2SyuNeMbdleub1cP4130_provenance.
- NP792205.RAG7PaNm28L5983xRxZQTWve5-NN2SyuNeMbdleub1cP4130_assertion wasDerivedFrom befree-20150227 NP792205.RAG7PaNm28L5983xRxZQTWve5-NN2SyuNeMbdleub1cP4130_provenance.
- NP792205.RAG7PaNm28L5983xRxZQTWve5-NN2SyuNeMbdleub1cP4130_assertion wasGeneratedBy ECO_0000203 NP792205.RAG7PaNm28L5983xRxZQTWve5-NN2SyuNeMbdleub1cP4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP792205.RAG7PaNm28L5983xRxZQTWve5-NN2SyuNeMbdleub1cP4130_provenance.