Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP130637.RARd_fUIOySKO9eD9HsaP74dv5GDOB8bLleKT50tg8C1U130_assertion> ?p ?o ?g. }
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- NP130637.RARd_fUIOySKO9eD9HsaP74dv5GDOB8bLleKT50tg8C1U130_assertion type Assertion NP130637.RARd_fUIOySKO9eD9HsaP74dv5GDOB8bLleKT50tg8C1U130_head.
- NP130637.RARd_fUIOySKO9eD9HsaP74dv5GDOB8bLleKT50tg8C1U130_assertion description "[A patient homozygous for A PINK1 mutation was characterized clinically/clinical and laboratory features, including SPECT and assessment of autonomic function, were indistinguishable from typical idiopathic Parkinson disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130637.RARd_fUIOySKO9eD9HsaP74dv5GDOB8bLleKT50tg8C1U130_provenance.
- NP130637.RARd_fUIOySKO9eD9HsaP74dv5GDOB8bLleKT50tg8C1U130_assertion evidence source_evidence_literature NP130637.RARd_fUIOySKO9eD9HsaP74dv5GDOB8bLleKT50tg8C1U130_provenance.
- NP130637.RARd_fUIOySKO9eD9HsaP74dv5GDOB8bLleKT50tg8C1U130_assertion SIO_000772 15955954 NP130637.RARd_fUIOySKO9eD9HsaP74dv5GDOB8bLleKT50tg8C1U130_provenance.
- NP130637.RARd_fUIOySKO9eD9HsaP74dv5GDOB8bLleKT50tg8C1U130_assertion wasDerivedFrom lhgdn-20090331 NP130637.RARd_fUIOySKO9eD9HsaP74dv5GDOB8bLleKT50tg8C1U130_provenance.
- NP130637.RARd_fUIOySKO9eD9HsaP74dv5GDOB8bLleKT50tg8C1U130_assertion wasGeneratedBy ECO_0000203 NP130637.RARd_fUIOySKO9eD9HsaP74dv5GDOB8bLleKT50tg8C1U130_provenance.