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- source_evidence_literature type ECO_0000212 NP615859.RAJ1lxoQXN978-DIDCMYo2e-B_SLpC6PA_NBtHExqaHdA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP615859.RAJ1lxoQXN978-DIDCMYo2e-B_SLpC6PA_NBtHExqaHdA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP615859.RAJ1lxoQXN978-DIDCMYo2e-B_SLpC6PA_NBtHExqaHdA130_provenance.
- NP615859.RAJ1lxoQXN978-DIDCMYo2e-B_SLpC6PA_NBtHExqaHdA130_assertion description "[These results indicate that polymorphisms in the OPA1 gene are associated with NTG and may be a marker for the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP615859.RAJ1lxoQXN978-DIDCMYo2e-B_SLpC6PA_NBtHExqaHdA130_provenance.
- NP615859.RAJ1lxoQXN978-DIDCMYo2e-B_SLpC6PA_NBtHExqaHdA130_assertion evidence source_evidence_literature NP615859.RAJ1lxoQXN978-DIDCMYo2e-B_SLpC6PA_NBtHExqaHdA130_provenance.
- NP615859.RAJ1lxoQXN978-DIDCMYo2e-B_SLpC6PA_NBtHExqaHdA130_assertion SIO_000772 11810296 NP615859.RAJ1lxoQXN978-DIDCMYo2e-B_SLpC6PA_NBtHExqaHdA130_provenance.
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- befree-20140225 importedOn "2014-02-25" NP615859.RAJ1lxoQXN978-DIDCMYo2e-B_SLpC6PA_NBtHExqaHdA130_provenance.