Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP193719.RAEUW7esFnzlJlgm1jCg4SaiDkWjFDR3tBCPuBP_FSSWQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP193719.RAEUW7esFnzlJlgm1jCg4SaiDkWjFDR3tBCPuBP_FSSWQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP193719.RAEUW7esFnzlJlgm1jCg4SaiDkWjFDR3tBCPuBP_FSSWQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP193719.RAEUW7esFnzlJlgm1jCg4SaiDkWjFDR3tBCPuBP_FSSWQ130_provenance.
- NP193719.RAEUW7esFnzlJlgm1jCg4SaiDkWjFDR3tBCPuBP_FSSWQ130_assertion description "[Carriers of parkin mutations are clinically indistinguishable from other patients with young-onset Parkinson disease (PD) on an individual basis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193719.RAEUW7esFnzlJlgm1jCg4SaiDkWjFDR3tBCPuBP_FSSWQ130_provenance.
- NP193719.RAEUW7esFnzlJlgm1jCg4SaiDkWjFDR3tBCPuBP_FSSWQ130_assertion evidence source_evidence_literature NP193719.RAEUW7esFnzlJlgm1jCg4SaiDkWjFDR3tBCPuBP_FSSWQ130_provenance.
- NP193719.RAEUW7esFnzlJlgm1jCg4SaiDkWjFDR3tBCPuBP_FSSWQ130_assertion SIO_000772 18987353 NP193719.RAEUW7esFnzlJlgm1jCg4SaiDkWjFDR3tBCPuBP_FSSWQ130_provenance.
- NP193719.RAEUW7esFnzlJlgm1jCg4SaiDkWjFDR3tBCPuBP_FSSWQ130_assertion wasDerivedFrom lhgdn-20090331 NP193719.RAEUW7esFnzlJlgm1jCg4SaiDkWjFDR3tBCPuBP_FSSWQ130_provenance.
- NP193719.RAEUW7esFnzlJlgm1jCg4SaiDkWjFDR3tBCPuBP_FSSWQ130_assertion wasGeneratedBy ECO_0000203 NP193719.RAEUW7esFnzlJlgm1jCg4SaiDkWjFDR3tBCPuBP_FSSWQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP193719.RAEUW7esFnzlJlgm1jCg4SaiDkWjFDR3tBCPuBP_FSSWQ130_provenance.