Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP717837.RA3pzCrqVKw-hAw41O0TM9_qssBkiXwkKbpAoSK4bzQTI130_assertion> ?p ?o ?g. }
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- NP717837.RA3pzCrqVKw-hAw41O0TM9_qssBkiXwkKbpAoSK4bzQTI130_assertion type Assertion NP717837.RA3pzCrqVKw-hAw41O0TM9_qssBkiXwkKbpAoSK4bzQTI130_head.
- NP717837.RA3pzCrqVKw-hAw41O0TM9_qssBkiXwkKbpAoSK4bzQTI130_assertion description "[Mutations in the ATP13A2 (PARK9) and FBXO7 (PARK15) genes are linked to different forms of autosomal recessive juvenile-onset neurodegenerative diseases with overlapping phenotypes, including levodopa-responsive parkinsonism, pyramidal disturbances, cognitive decline, and supranuclear gaze disturbance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717837.RA3pzCrqVKw-hAw41O0TM9_qssBkiXwkKbpAoSK4bzQTI130_provenance.
- NP717837.RA3pzCrqVKw-hAw41O0TM9_qssBkiXwkKbpAoSK4bzQTI130_assertion evidence source_evidence_literature NP717837.RA3pzCrqVKw-hAw41O0TM9_qssBkiXwkKbpAoSK4bzQTI130_provenance.
- NP717837.RA3pzCrqVKw-hAw41O0TM9_qssBkiXwkKbpAoSK4bzQTI130_assertion SIO_000772 20853184 NP717837.RA3pzCrqVKw-hAw41O0TM9_qssBkiXwkKbpAoSK4bzQTI130_provenance.
- NP717837.RA3pzCrqVKw-hAw41O0TM9_qssBkiXwkKbpAoSK4bzQTI130_assertion wasDerivedFrom befree-20140225 NP717837.RA3pzCrqVKw-hAw41O0TM9_qssBkiXwkKbpAoSK4bzQTI130_provenance.
- NP717837.RA3pzCrqVKw-hAw41O0TM9_qssBkiXwkKbpAoSK4bzQTI130_assertion wasGeneratedBy ECO_0000203 NP717837.RA3pzCrqVKw-hAw41O0TM9_qssBkiXwkKbpAoSK4bzQTI130_provenance.