Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- 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." provenance.
- 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." provenance.
- NP864112.RAsxn18kqkJTtY7PB6gNFehqalxahaSrvvCSsC7B8JIek130_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." NP864112.RAsxn18kqkJTtY7PB6gNFehqalxahaSrvvCSsC7B8JIek130_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.
- NP709613.RALJMY8peRTKN6JN5RfvIeT7tfnxkgOA9u9BH_3ZFKQQA130_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." NP709613.RALJMY8peRTKN6JN5RfvIeT7tfnxkgOA9u9BH_3ZFKQQA130_provenance.