Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP140666.RAlNTOkv_nsfl7C0mZ-TmMbLN9aFCBwVcagRzoB_0oUZw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP140666.RAlNTOkv_nsfl7C0mZ-TmMbLN9aFCBwVcagRzoB_0oUZw130_assertion type Assertion NP140666.RAlNTOkv_nsfl7C0mZ-TmMbLN9aFCBwVcagRzoB_0oUZw130_head.
- NP140666.RAlNTOkv_nsfl7C0mZ-TmMbLN9aFCBwVcagRzoB_0oUZw130_assertion description "[Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: phenotypic characterization and frequency of SNCA, PRKN, PINK1, and LRRK2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP140666.RAlNTOkv_nsfl7C0mZ-TmMbLN9aFCBwVcagRzoB_0oUZw130_provenance.
- NP140666.RAlNTOkv_nsfl7C0mZ-TmMbLN9aFCBwVcagRzoB_0oUZw130_assertion evidence source_evidence_literature NP140666.RAlNTOkv_nsfl7C0mZ-TmMbLN9aFCBwVcagRzoB_0oUZw130_provenance.
- NP140666.RAlNTOkv_nsfl7C0mZ-TmMbLN9aFCBwVcagRzoB_0oUZw130_assertion SIO_000772 19205068 NP140666.RAlNTOkv_nsfl7C0mZ-TmMbLN9aFCBwVcagRzoB_0oUZw130_provenance.
- NP140666.RAlNTOkv_nsfl7C0mZ-TmMbLN9aFCBwVcagRzoB_0oUZw130_assertion wasDerivedFrom gad-20150221 NP140666.RAlNTOkv_nsfl7C0mZ-TmMbLN9aFCBwVcagRzoB_0oUZw130_provenance.
- NP140666.RAlNTOkv_nsfl7C0mZ-TmMbLN9aFCBwVcagRzoB_0oUZw130_assertion wasGeneratedBy ECO_0000203 NP140666.RAlNTOkv_nsfl7C0mZ-TmMbLN9aFCBwVcagRzoB_0oUZw130_provenance.