Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP499436.RAdEpTNHRJxqDlqnFyCtDSinsFM2y7E7RBtu5c2FhQY5o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP499436.RAdEpTNHRJxqDlqnFyCtDSinsFM2y7E7RBtu5c2FhQY5o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP499436.RAdEpTNHRJxqDlqnFyCtDSinsFM2y7E7RBtu5c2FhQY5o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP499436.RAdEpTNHRJxqDlqnFyCtDSinsFM2y7E7RBtu5c2FhQY5o130_provenance.
- NP499436.RAdEpTNHRJxqDlqnFyCtDSinsFM2y7E7RBtu5c2FhQY5o130_assertion description "[Mutations in the PINK1 gene cause autosomal recessive parkinsonism characterized by early onset and a variable phenotypic presentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499436.RAdEpTNHRJxqDlqnFyCtDSinsFM2y7E7RBtu5c2FhQY5o130_provenance.
- NP499436.RAdEpTNHRJxqDlqnFyCtDSinsFM2y7E7RBtu5c2FhQY5o130_assertion evidence source_evidence_literature NP499436.RAdEpTNHRJxqDlqnFyCtDSinsFM2y7E7RBtu5c2FhQY5o130_provenance.
- NP499436.RAdEpTNHRJxqDlqnFyCtDSinsFM2y7E7RBtu5c2FhQY5o130_assertion SIO_000772 15955954 NP499436.RAdEpTNHRJxqDlqnFyCtDSinsFM2y7E7RBtu5c2FhQY5o130_provenance.
- NP499436.RAdEpTNHRJxqDlqnFyCtDSinsFM2y7E7RBtu5c2FhQY5o130_assertion wasDerivedFrom befree-2016 NP499436.RAdEpTNHRJxqDlqnFyCtDSinsFM2y7E7RBtu5c2FhQY5o130_provenance.
- NP499436.RAdEpTNHRJxqDlqnFyCtDSinsFM2y7E7RBtu5c2FhQY5o130_assertion wasGeneratedBy ECO_0000203 NP499436.RAdEpTNHRJxqDlqnFyCtDSinsFM2y7E7RBtu5c2FhQY5o130_provenance.
- befree-2016 importedOn "2016-02-19" NP499436.RAdEpTNHRJxqDlqnFyCtDSinsFM2y7E7RBtu5c2FhQY5o130_provenance.