Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP969849.RAyW2yKQfj17nIcndiPkRbSuNTHkXBAE3h4ZzcZw_IMv4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP969849.RAyW2yKQfj17nIcndiPkRbSuNTHkXBAE3h4ZzcZw_IMv4130_assertion type Assertion NP969849.RAyW2yKQfj17nIcndiPkRbSuNTHkXBAE3h4ZzcZw_IMv4130_head.
- NP969849.RAyW2yKQfj17nIcndiPkRbSuNTHkXBAE3h4ZzcZw_IMv4130_assertion description "[Mutations in lysosomal membrane protein ATP13A2 (PARK9) cause familial Kufor-Rakeb syndrome characterized by early-onset parkinsonism, pyramidal degeneration and dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP969849.RAyW2yKQfj17nIcndiPkRbSuNTHkXBAE3h4ZzcZw_IMv4130_provenance.
- NP969849.RAyW2yKQfj17nIcndiPkRbSuNTHkXBAE3h4ZzcZw_IMv4130_assertion evidence source_evidence_literature NP969849.RAyW2yKQfj17nIcndiPkRbSuNTHkXBAE3h4ZzcZw_IMv4130_provenance.
- NP969849.RAyW2yKQfj17nIcndiPkRbSuNTHkXBAE3h4ZzcZw_IMv4130_assertion SIO_000772 22442086 NP969849.RAyW2yKQfj17nIcndiPkRbSuNTHkXBAE3h4ZzcZw_IMv4130_provenance.
- NP969849.RAyW2yKQfj17nIcndiPkRbSuNTHkXBAE3h4ZzcZw_IMv4130_assertion wasDerivedFrom befree-2016 NP969849.RAyW2yKQfj17nIcndiPkRbSuNTHkXBAE3h4ZzcZw_IMv4130_provenance.
- NP969849.RAyW2yKQfj17nIcndiPkRbSuNTHkXBAE3h4ZzcZw_IMv4130_assertion wasGeneratedBy ECO_0000203 NP969849.RAyW2yKQfj17nIcndiPkRbSuNTHkXBAE3h4ZzcZw_IMv4130_provenance.