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- source_evidence_literature type ECO_0000212 NP645210.RAyR_m1H_QvzkSVI_oZptVWXnNDm3DXiY_4MUUxlhmAfA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP645210.RAyR_m1H_QvzkSVI_oZptVWXnNDm3DXiY_4MUUxlhmAfA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP645210.RAyR_m1H_QvzkSVI_oZptVWXnNDm3DXiY_4MUUxlhmAfA130_provenance.
- NP645210.RAyR_m1H_QvzkSVI_oZptVWXnNDm3DXiY_4MUUxlhmAfA130_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." NP645210.RAyR_m1H_QvzkSVI_oZptVWXnNDm3DXiY_4MUUxlhmAfA130_provenance.
- NP645210.RAyR_m1H_QvzkSVI_oZptVWXnNDm3DXiY_4MUUxlhmAfA130_assertion evidence source_evidence_literature NP645210.RAyR_m1H_QvzkSVI_oZptVWXnNDm3DXiY_4MUUxlhmAfA130_provenance.
- NP645210.RAyR_m1H_QvzkSVI_oZptVWXnNDm3DXiY_4MUUxlhmAfA130_assertion SIO_000772 18079691 NP645210.RAyR_m1H_QvzkSVI_oZptVWXnNDm3DXiY_4MUUxlhmAfA130_provenance.
- NP645210.RAyR_m1H_QvzkSVI_oZptVWXnNDm3DXiY_4MUUxlhmAfA130_assertion wasDerivedFrom befree-2016 NP645210.RAyR_m1H_QvzkSVI_oZptVWXnNDm3DXiY_4MUUxlhmAfA130_provenance.
- NP645210.RAyR_m1H_QvzkSVI_oZptVWXnNDm3DXiY_4MUUxlhmAfA130_assertion wasGeneratedBy ECO_0000203 NP645210.RAyR_m1H_QvzkSVI_oZptVWXnNDm3DXiY_4MUUxlhmAfA130_provenance.
- befree-2016 importedOn "2016-02-19" NP645210.RAyR_m1H_QvzkSVI_oZptVWXnNDm3DXiY_4MUUxlhmAfA130_provenance.