Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1038090.RAA88Ghjob2y90fXQUn2azTqgqUQy3vQ4Nb1w1OKCfJJw130_assertion> ?p ?o ?g. }
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- NP1038090.RAA88Ghjob2y90fXQUn2azTqgqUQy3vQ4Nb1w1OKCfJJw130_assertion type Assertion NP1038090.RAA88Ghjob2y90fXQUn2azTqgqUQy3vQ4Nb1w1OKCfJJw130_head.
- NP1038090.RAA88Ghjob2y90fXQUn2azTqgqUQy3vQ4Nb1w1OKCfJJw130_assertion description "[Mutation in the human PTEN-induced protein kinase 1 (PINK1) gene is responsible for the second most common form of recessive Parkinson disease (PD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1038090.RAA88Ghjob2y90fXQUn2azTqgqUQy3vQ4Nb1w1OKCfJJw130_provenance.
- NP1038090.RAA88Ghjob2y90fXQUn2azTqgqUQy3vQ4Nb1w1OKCfJJw130_assertion evidence source_evidence_literature NP1038090.RAA88Ghjob2y90fXQUn2azTqgqUQy3vQ4Nb1w1OKCfJJw130_provenance.
- NP1038090.RAA88Ghjob2y90fXQUn2azTqgqUQy3vQ4Nb1w1OKCfJJw130_assertion SIO_000772 23261939 NP1038090.RAA88Ghjob2y90fXQUn2azTqgqUQy3vQ4Nb1w1OKCfJJw130_provenance.
- NP1038090.RAA88Ghjob2y90fXQUn2azTqgqUQy3vQ4Nb1w1OKCfJJw130_assertion wasDerivedFrom befree-2016 NP1038090.RAA88Ghjob2y90fXQUn2azTqgqUQy3vQ4Nb1w1OKCfJJw130_provenance.
- NP1038090.RAA88Ghjob2y90fXQUn2azTqgqUQy3vQ4Nb1w1OKCfJJw130_assertion wasGeneratedBy ECO_0000203 NP1038090.RAA88Ghjob2y90fXQUn2azTqgqUQy3vQ4Nb1w1OKCfJJw130_provenance.