Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP130705.RADlJqNjsgdCx0qOOtRyEXLyb8GnHKAZtDbnv6KfduD74130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP130705.RADlJqNjsgdCx0qOOtRyEXLyb8GnHKAZtDbnv6KfduD74130_assertion type Assertion NP130705.RADlJqNjsgdCx0qOOtRyEXLyb8GnHKAZtDbnv6KfduD74130_head.
- NP130705.RADlJqNjsgdCx0qOOtRyEXLyb8GnHKAZtDbnv6KfduD74130_assertion description "[A rare variant (AL746Thr) of the ATP13A2 was associated with an increased risk of Parkinson disease among ethnic Chinese in Asia/studies are needed to clarify the functional role of this genetic risk factor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130705.RADlJqNjsgdCx0qOOtRyEXLyb8GnHKAZtDbnv6KfduD74130_provenance.
- NP130705.RADlJqNjsgdCx0qOOtRyEXLyb8GnHKAZtDbnv6KfduD74130_assertion evidence source_evidence_literature NP130705.RADlJqNjsgdCx0qOOtRyEXLyb8GnHKAZtDbnv6KfduD74130_provenance.
- NP130705.RADlJqNjsgdCx0qOOtRyEXLyb8GnHKAZtDbnv6KfduD74130_assertion SIO_000772 19015489 NP130705.RADlJqNjsgdCx0qOOtRyEXLyb8GnHKAZtDbnv6KfduD74130_provenance.
- NP130705.RADlJqNjsgdCx0qOOtRyEXLyb8GnHKAZtDbnv6KfduD74130_assertion wasDerivedFrom lhgdn-20090331 NP130705.RADlJqNjsgdCx0qOOtRyEXLyb8GnHKAZtDbnv6KfduD74130_provenance.
- NP130705.RADlJqNjsgdCx0qOOtRyEXLyb8GnHKAZtDbnv6KfduD74130_assertion wasGeneratedBy ECO_0000203 NP130705.RADlJqNjsgdCx0qOOtRyEXLyb8GnHKAZtDbnv6KfduD74130_provenance.