Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP111036.RAtZZ8OuF_J2i85x3btzDzWNQ4JAfEFnltZLd3zX_tZac130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP111036.RAtZZ8OuF_J2i85x3btzDzWNQ4JAfEFnltZLd3zX_tZac130_assertion type Assertion NP111036.RAtZZ8OuF_J2i85x3btzDzWNQ4JAfEFnltZLd3zX_tZac130_head.
- NP111036.RAtZZ8OuF_J2i85x3btzDzWNQ4JAfEFnltZLd3zX_tZac130_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." NP111036.RAtZZ8OuF_J2i85x3btzDzWNQ4JAfEFnltZLd3zX_tZac130_provenance.
- NP111036.RAtZZ8OuF_J2i85x3btzDzWNQ4JAfEFnltZLd3zX_tZac130_assertion evidence source_evidence_literature NP111036.RAtZZ8OuF_J2i85x3btzDzWNQ4JAfEFnltZLd3zX_tZac130_provenance.
- NP111036.RAtZZ8OuF_J2i85x3btzDzWNQ4JAfEFnltZLd3zX_tZac130_assertion SIO_000772 17055324 NP111036.RAtZZ8OuF_J2i85x3btzDzWNQ4JAfEFnltZLd3zX_tZac130_provenance.
- NP111036.RAtZZ8OuF_J2i85x3btzDzWNQ4JAfEFnltZLd3zX_tZac130_assertion wasDerivedFrom lhgdn-20090331 NP111036.RAtZZ8OuF_J2i85x3btzDzWNQ4JAfEFnltZLd3zX_tZac130_provenance.
- NP111036.RAtZZ8OuF_J2i85x3btzDzWNQ4JAfEFnltZLd3zX_tZac130_assertion wasGeneratedBy ECO_0000203 NP111036.RAtZZ8OuF_J2i85x3btzDzWNQ4JAfEFnltZLd3zX_tZac130_provenance.