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- source_evidence_literature type ECO_0000212 NP362877.RAqxuB8UxZ8W6bkEetc4S52_TRuxt4vavuRhPfN7SQxEM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP362877.RAqxuB8UxZ8W6bkEetc4S52_TRuxt4vavuRhPfN7SQxEM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP362877.RAqxuB8UxZ8W6bkEetc4S52_TRuxt4vavuRhPfN7SQxEM130_provenance.
- NP362877.RAqxuB8UxZ8W6bkEetc4S52_TRuxt4vavuRhPfN7SQxEM130_assertion description "[Mutations in the DYT1 gene can cause focal dystonia, and an association with a polymorphism in the D5 receptor gene (DRD5) has been reported but not confirmed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP362877.RAqxuB8UxZ8W6bkEetc4S52_TRuxt4vavuRhPfN7SQxEM130_provenance.
- NP362877.RAqxuB8UxZ8W6bkEetc4S52_TRuxt4vavuRhPfN7SQxEM130_assertion evidence source_evidence_literature NP362877.RAqxuB8UxZ8W6bkEetc4S52_TRuxt4vavuRhPfN7SQxEM130_provenance.
- NP362877.RAqxuB8UxZ8W6bkEetc4S52_TRuxt4vavuRhPfN7SQxEM130_assertion SIO_000772 14581671 NP362877.RAqxuB8UxZ8W6bkEetc4S52_TRuxt4vavuRhPfN7SQxEM130_provenance.
- NP362877.RAqxuB8UxZ8W6bkEetc4S52_TRuxt4vavuRhPfN7SQxEM130_assertion wasDerivedFrom befree-20150227 NP362877.RAqxuB8UxZ8W6bkEetc4S52_TRuxt4vavuRhPfN7SQxEM130_provenance.
- NP362877.RAqxuB8UxZ8W6bkEetc4S52_TRuxt4vavuRhPfN7SQxEM130_assertion wasGeneratedBy ECO_0000203 NP362877.RAqxuB8UxZ8W6bkEetc4S52_TRuxt4vavuRhPfN7SQxEM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP362877.RAqxuB8UxZ8W6bkEetc4S52_TRuxt4vavuRhPfN7SQxEM130_provenance.