Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP575514.RAuIW_1rDhdlewyEmOpU8wouVFHi1ADoQ1AvK8kJEzTdA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP575514.RAuIW_1rDhdlewyEmOpU8wouVFHi1ADoQ1AvK8kJEzTdA130_assertion type Assertion NP575514.RAuIW_1rDhdlewyEmOpU8wouVFHi1ADoQ1AvK8kJEzTdA130_head.
- NP575514.RAuIW_1rDhdlewyEmOpU8wouVFHi1ADoQ1AvK8kJEzTdA130_assertion description "[We genotyped eight known mutations in three clinic-based cohorts with Parkinsonism and found one homozygous p.L347P mutation in PINK1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP575514.RAuIW_1rDhdlewyEmOpU8wouVFHi1ADoQ1AvK8kJEzTdA130_provenance.
- NP575514.RAuIW_1rDhdlewyEmOpU8wouVFHi1ADoQ1AvK8kJEzTdA130_assertion evidence source_evidence_literature NP575514.RAuIW_1rDhdlewyEmOpU8wouVFHi1ADoQ1AvK8kJEzTdA130_provenance.
- NP575514.RAuIW_1rDhdlewyEmOpU8wouVFHi1ADoQ1AvK8kJEzTdA130_assertion SIO_000772 17055324 NP575514.RAuIW_1rDhdlewyEmOpU8wouVFHi1ADoQ1AvK8kJEzTdA130_provenance.
- NP575514.RAuIW_1rDhdlewyEmOpU8wouVFHi1ADoQ1AvK8kJEzTdA130_assertion wasDerivedFrom befree-2016 NP575514.RAuIW_1rDhdlewyEmOpU8wouVFHi1ADoQ1AvK8kJEzTdA130_provenance.
- NP575514.RAuIW_1rDhdlewyEmOpU8wouVFHi1ADoQ1AvK8kJEzTdA130_assertion wasGeneratedBy ECO_0000203 NP575514.RAuIW_1rDhdlewyEmOpU8wouVFHi1ADoQ1AvK8kJEzTdA130_provenance.