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- source_evidence_literature type ECO_0000212 NP645213.RAcUVM65JPOAnIuyj_7lMO-Ir6WQ6pZEVERxEzxRV2rxI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP645213.RAcUVM65JPOAnIuyj_7lMO-Ir6WQ6pZEVERxEzxRV2rxI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP645213.RAcUVM65JPOAnIuyj_7lMO-Ir6WQ6pZEVERxEzxRV2rxI130_provenance.
- NP645213.RAcUVM65JPOAnIuyj_7lMO-Ir6WQ6pZEVERxEzxRV2rxI130_assertion description "[Compared to PLEKHA1, HTRA1/LOC387715 genetic variations were independently and strongly associated with exudative AMD in the French population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP645213.RAcUVM65JPOAnIuyj_7lMO-Ir6WQ6pZEVERxEzxRV2rxI130_provenance.
- NP645213.RAcUVM65JPOAnIuyj_7lMO-Ir6WQ6pZEVERxEzxRV2rxI130_assertion evidence source_evidence_literature NP645213.RAcUVM65JPOAnIuyj_7lMO-Ir6WQ6pZEVERxEzxRV2rxI130_provenance.
- NP645213.RAcUVM65JPOAnIuyj_7lMO-Ir6WQ6pZEVERxEzxRV2rxI130_assertion SIO_000772 18079691 NP645213.RAcUVM65JPOAnIuyj_7lMO-Ir6WQ6pZEVERxEzxRV2rxI130_provenance.
- NP645213.RAcUVM65JPOAnIuyj_7lMO-Ir6WQ6pZEVERxEzxRV2rxI130_assertion wasDerivedFrom befree-2016 NP645213.RAcUVM65JPOAnIuyj_7lMO-Ir6WQ6pZEVERxEzxRV2rxI130_provenance.
- NP645213.RAcUVM65JPOAnIuyj_7lMO-Ir6WQ6pZEVERxEzxRV2rxI130_assertion wasGeneratedBy ECO_0000203 NP645213.RAcUVM65JPOAnIuyj_7lMO-Ir6WQ6pZEVERxEzxRV2rxI130_provenance.
- befree-2016 importedOn "2016-02-19" NP645213.RAcUVM65JPOAnIuyj_7lMO-Ir6WQ6pZEVERxEzxRV2rxI130_provenance.