Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP967250.RAWCKHoIPRnICJD-rRPNwX91X3xDiZu_ObO1oIuecjXHg130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP967250.RAWCKHoIPRnICJD-rRPNwX91X3xDiZu_ObO1oIuecjXHg130_assertion type Assertion NP967250.RAWCKHoIPRnICJD-rRPNwX91X3xDiZu_ObO1oIuecjXHg130_head.
- NP967250.RAWCKHoIPRnICJD-rRPNwX91X3xDiZu_ObO1oIuecjXHg130_assertion description "[We screened the most common LRRK2 mutation (p.G2019S) in a series of 180 consecutive patients clinically diagnosed with Alzheimer Disease (AD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP967250.RAWCKHoIPRnICJD-rRPNwX91X3xDiZu_ObO1oIuecjXHg130_provenance.
- NP967250.RAWCKHoIPRnICJD-rRPNwX91X3xDiZu_ObO1oIuecjXHg130_assertion evidence source_evidence_literature NP967250.RAWCKHoIPRnICJD-rRPNwX91X3xDiZu_ObO1oIuecjXHg130_provenance.
- NP967250.RAWCKHoIPRnICJD-rRPNwX91X3xDiZu_ObO1oIuecjXHg130_assertion SIO_000772 19822953 NP967250.RAWCKHoIPRnICJD-rRPNwX91X3xDiZu_ObO1oIuecjXHg130_provenance.
- NP967250.RAWCKHoIPRnICJD-rRPNwX91X3xDiZu_ObO1oIuecjXHg130_assertion wasDerivedFrom befree-20150227 NP967250.RAWCKHoIPRnICJD-rRPNwX91X3xDiZu_ObO1oIuecjXHg130_provenance.
- NP967250.RAWCKHoIPRnICJD-rRPNwX91X3xDiZu_ObO1oIuecjXHg130_assertion wasGeneratedBy ECO_0000203 NP967250.RAWCKHoIPRnICJD-rRPNwX91X3xDiZu_ObO1oIuecjXHg130_provenance.