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- source_evidence_literature type ECO_0000212 NP709615.RAf9qIlP-qahggPLpwwww4BgD2w6ilZ_pp5hjFeFft260130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP709615.RAf9qIlP-qahggPLpwwww4BgD2w6ilZ_pp5hjFeFft260130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP709615.RAf9qIlP-qahggPLpwwww4BgD2w6ilZ_pp5hjFeFft260130_provenance.
- NP709615.RAf9qIlP-qahggPLpwwww4BgD2w6ilZ_pp5hjFeFft260130_assertion description "[In rare incidences familial forms of early-onset parkinsonism occur, and when recessively inherited, cases are often explained by mutations in either the parkin (PARK2) or PINK1 (PARK6) gene or on exceptional occasions the DJ-1 (PARK7) or ATP13A2 (PARK9) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP709615.RAf9qIlP-qahggPLpwwww4BgD2w6ilZ_pp5hjFeFft260130_provenance.
- NP709615.RAf9qIlP-qahggPLpwwww4BgD2w6ilZ_pp5hjFeFft260130_assertion evidence source_evidence_literature NP709615.RAf9qIlP-qahggPLpwwww4BgD2w6ilZ_pp5hjFeFft260130_provenance.
- NP709615.RAf9qIlP-qahggPLpwwww4BgD2w6ilZ_pp5hjFeFft260130_assertion SIO_000772 19087301 NP709615.RAf9qIlP-qahggPLpwwww4BgD2w6ilZ_pp5hjFeFft260130_provenance.
- NP709615.RAf9qIlP-qahggPLpwwww4BgD2w6ilZ_pp5hjFeFft260130_assertion wasDerivedFrom befree-2016 NP709615.RAf9qIlP-qahggPLpwwww4BgD2w6ilZ_pp5hjFeFft260130_provenance.
- NP709615.RAf9qIlP-qahggPLpwwww4BgD2w6ilZ_pp5hjFeFft260130_assertion wasGeneratedBy ECO_0000203 NP709615.RAf9qIlP-qahggPLpwwww4BgD2w6ilZ_pp5hjFeFft260130_provenance.
- befree-2016 importedOn "2016-02-19" NP709615.RAf9qIlP-qahggPLpwwww4BgD2w6ilZ_pp5hjFeFft260130_provenance.