Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1260243.RAUi_hU64sD4kkh8LNv7xN5wtXYtX5uGlaWbgNh1EtrmY130_assertion> ?p ?o ?g. }
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- NP1260243.RAUi_hU64sD4kkh8LNv7xN5wtXYtX5uGlaWbgNh1EtrmY130_assertion type Assertion NP1260243.RAUi_hU64sD4kkh8LNv7xN5wtXYtX5uGlaWbgNh1EtrmY130_head.
- NP1260243.RAUi_hU64sD4kkh8LNv7xN5wtXYtX5uGlaWbgNh1EtrmY130_assertion description "[Other entities entailing dystonia-parkinsonism include dopamine transporter deficiency syndrome (SLC63 mutations); dopa-responsive dystonias; young-onset parkinsonism (PARKIN, PINK1 and DJ-1 mutations); PRKRA mutations; and X-linked TAF1 mutations, which rarely can also manifest in women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260243.RAUi_hU64sD4kkh8LNv7xN5wtXYtX5uGlaWbgNh1EtrmY130_provenance.
- NP1260243.RAUi_hU64sD4kkh8LNv7xN5wtXYtX5uGlaWbgNh1EtrmY130_assertion evidence source_evidence_literature NP1260243.RAUi_hU64sD4kkh8LNv7xN5wtXYtX5uGlaWbgNh1EtrmY130_provenance.
- NP1260243.RAUi_hU64sD4kkh8LNv7xN5wtXYtX5uGlaWbgNh1EtrmY130_assertion SIO_000772 25643588 NP1260243.RAUi_hU64sD4kkh8LNv7xN5wtXYtX5uGlaWbgNh1EtrmY130_provenance.
- NP1260243.RAUi_hU64sD4kkh8LNv7xN5wtXYtX5uGlaWbgNh1EtrmY130_assertion wasDerivedFrom befree-2016 NP1260243.RAUi_hU64sD4kkh8LNv7xN5wtXYtX5uGlaWbgNh1EtrmY130_provenance.
- NP1260243.RAUi_hU64sD4kkh8LNv7xN5wtXYtX5uGlaWbgNh1EtrmY130_assertion wasGeneratedBy ECO_0000203 NP1260243.RAUi_hU64sD4kkh8LNv7xN5wtXYtX5uGlaWbgNh1EtrmY130_provenance.