Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP356419.RAyuBBnDYctYYg3Dwu1Ljkf1itaiv7O_j_POQqB7K-UjM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP356419.RAyuBBnDYctYYg3Dwu1Ljkf1itaiv7O_j_POQqB7K-UjM130_assertion type Assertion NP356419.RAyuBBnDYctYYg3Dwu1Ljkf1itaiv7O_j_POQqB7K-UjM130_head.
- NP356419.RAyuBBnDYctYYg3Dwu1Ljkf1itaiv7O_j_POQqB7K-UjM130_assertion description "[Mutations in ATP13A2 (PARK9), encoding a lysosomal P-type ATPase, are associated with both Kufor-Rakeb syndrome (KRS) and neuronal ceroid lipofuscinosis (NCL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP356419.RAyuBBnDYctYYg3Dwu1Ljkf1itaiv7O_j_POQqB7K-UjM130_provenance.
- NP356419.RAyuBBnDYctYYg3Dwu1Ljkf1itaiv7O_j_POQqB7K-UjM130_assertion evidence source_evidence_literature NP356419.RAyuBBnDYctYYg3Dwu1Ljkf1itaiv7O_j_POQqB7K-UjM130_provenance.
- NP356419.RAyuBBnDYctYYg3Dwu1Ljkf1itaiv7O_j_POQqB7K-UjM130_assertion SIO_000772 23393156 NP356419.RAyuBBnDYctYYg3Dwu1Ljkf1itaiv7O_j_POQqB7K-UjM130_provenance.
- NP356419.RAyuBBnDYctYYg3Dwu1Ljkf1itaiv7O_j_POQqB7K-UjM130_assertion wasDerivedFrom befree-20150227 NP356419.RAyuBBnDYctYYg3Dwu1Ljkf1itaiv7O_j_POQqB7K-UjM130_provenance.
- NP356419.RAyuBBnDYctYYg3Dwu1Ljkf1itaiv7O_j_POQqB7K-UjM130_assertion wasGeneratedBy ECO_0000203 NP356419.RAyuBBnDYctYYg3Dwu1Ljkf1itaiv7O_j_POQqB7K-UjM130_provenance.