Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP938909.RACxyePOVZfCoJA0Y0WgxoDeQ2hqgtB7VtyLpxLXn7MaE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP938909.RACxyePOVZfCoJA0Y0WgxoDeQ2hqgtB7VtyLpxLXn7MaE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP938909.RACxyePOVZfCoJA0Y0WgxoDeQ2hqgtB7VtyLpxLXn7MaE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP938909.RACxyePOVZfCoJA0Y0WgxoDeQ2hqgtB7VtyLpxLXn7MaE130_provenance.
- NP938909.RACxyePOVZfCoJA0Y0WgxoDeQ2hqgtB7VtyLpxLXn7MaE130_assertion description "[Compound heterozygous parkin mutations (EX 3_6 del and EX 5 del) caused EOPD in this family, but the A265G variant in the HS1BP3 gene, previously considered to be responsible for ET, was probably not pathogenically related to the ET in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP938909.RACxyePOVZfCoJA0Y0WgxoDeQ2hqgtB7VtyLpxLXn7MaE130_provenance.
- NP938909.RACxyePOVZfCoJA0Y0WgxoDeQ2hqgtB7VtyLpxLXn7MaE130_assertion evidence source_evidence_literature NP938909.RACxyePOVZfCoJA0Y0WgxoDeQ2hqgtB7VtyLpxLXn7MaE130_provenance.
- NP938909.RACxyePOVZfCoJA0Y0WgxoDeQ2hqgtB7VtyLpxLXn7MaE130_assertion SIO_000772 17353387 NP938909.RACxyePOVZfCoJA0Y0WgxoDeQ2hqgtB7VtyLpxLXn7MaE130_provenance.
- NP938909.RACxyePOVZfCoJA0Y0WgxoDeQ2hqgtB7VtyLpxLXn7MaE130_assertion wasDerivedFrom befree-20150227 NP938909.RACxyePOVZfCoJA0Y0WgxoDeQ2hqgtB7VtyLpxLXn7MaE130_provenance.
- NP938909.RACxyePOVZfCoJA0Y0WgxoDeQ2hqgtB7VtyLpxLXn7MaE130_assertion wasGeneratedBy ECO_0000203 NP938909.RACxyePOVZfCoJA0Y0WgxoDeQ2hqgtB7VtyLpxLXn7MaE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP938909.RACxyePOVZfCoJA0Y0WgxoDeQ2hqgtB7VtyLpxLXn7MaE130_provenance.