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- source_evidence_literature type ECO_0000212 NP393124.RAVehR4_L7MILx_C75gbO_hWxF0htfnXcYgTtU0cmHp4Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP393124.RAVehR4_L7MILx_C75gbO_hWxF0htfnXcYgTtU0cmHp4Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP393124.RAVehR4_L7MILx_C75gbO_hWxF0htfnXcYgTtU0cmHp4Q130_provenance.
- NP393124.RAVehR4_L7MILx_C75gbO_hWxF0htfnXcYgTtU0cmHp4Q130_assertion description "[The allele frequencies of AGT point mutation at 235 (M235T) was significantly higher in DM nephropathy but the genotypic frequencies were not.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP393124.RAVehR4_L7MILx_C75gbO_hWxF0htfnXcYgTtU0cmHp4Q130_provenance.
- NP393124.RAVehR4_L7MILx_C75gbO_hWxF0htfnXcYgTtU0cmHp4Q130_assertion evidence source_evidence_literature NP393124.RAVehR4_L7MILx_C75gbO_hWxF0htfnXcYgTtU0cmHp4Q130_provenance.
- NP393124.RAVehR4_L7MILx_C75gbO_hWxF0htfnXcYgTtU0cmHp4Q130_assertion SIO_000772 12728975 NP393124.RAVehR4_L7MILx_C75gbO_hWxF0htfnXcYgTtU0cmHp4Q130_provenance.
- NP393124.RAVehR4_L7MILx_C75gbO_hWxF0htfnXcYgTtU0cmHp4Q130_assertion wasDerivedFrom befree-2016 NP393124.RAVehR4_L7MILx_C75gbO_hWxF0htfnXcYgTtU0cmHp4Q130_provenance.
- NP393124.RAVehR4_L7MILx_C75gbO_hWxF0htfnXcYgTtU0cmHp4Q130_assertion wasGeneratedBy ECO_0000203 NP393124.RAVehR4_L7MILx_C75gbO_hWxF0htfnXcYgTtU0cmHp4Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP393124.RAVehR4_L7MILx_C75gbO_hWxF0htfnXcYgTtU0cmHp4Q130_provenance.