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- source_evidence_literature type ECO_0000212 NP212618.RAShsZC2nCehFo4RMlAW-t1UU5YeVXhHyorSepb0itfys130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP212618.RAShsZC2nCehFo4RMlAW-t1UU5YeVXhHyorSepb0itfys130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP212618.RAShsZC2nCehFo4RMlAW-t1UU5YeVXhHyorSepb0itfys130_provenance.
- NP212618.RAShsZC2nCehFo4RMlAW-t1UU5YeVXhHyorSepb0itfys130_assertion description "[the AGTR1 A1166C and the NOS3 G894T polymorphisms are associated with silent white matter lesions in the subcortical area in essential hypertension ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP212618.RAShsZC2nCehFo4RMlAW-t1UU5YeVXhHyorSepb0itfys130_provenance.
- NP212618.RAShsZC2nCehFo4RMlAW-t1UU5YeVXhHyorSepb0itfys130_assertion evidence source_evidence_literature NP212618.RAShsZC2nCehFo4RMlAW-t1UU5YeVXhHyorSepb0itfys130_provenance.
- NP212618.RAShsZC2nCehFo4RMlAW-t1UU5YeVXhHyorSepb0itfys130_assertion SIO_000772 16109907 NP212618.RAShsZC2nCehFo4RMlAW-t1UU5YeVXhHyorSepb0itfys130_provenance.
- NP212618.RAShsZC2nCehFo4RMlAW-t1UU5YeVXhHyorSepb0itfys130_assertion wasDerivedFrom lhgdn-20090331 NP212618.RAShsZC2nCehFo4RMlAW-t1UU5YeVXhHyorSepb0itfys130_provenance.
- NP212618.RAShsZC2nCehFo4RMlAW-t1UU5YeVXhHyorSepb0itfys130_assertion wasGeneratedBy ECO_0000203 NP212618.RAShsZC2nCehFo4RMlAW-t1UU5YeVXhHyorSepb0itfys130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP212618.RAShsZC2nCehFo4RMlAW-t1UU5YeVXhHyorSepb0itfys130_provenance.