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- source_evidence_literature type ECO_0000212 NP768965.RA3xX33O34SrYR3V7IV6cnwpjkVtfNcXhujANcH8cQ54w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768965.RA3xX33O34SrYR3V7IV6cnwpjkVtfNcXhujANcH8cQ54w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768965.RA3xX33O34SrYR3V7IV6cnwpjkVtfNcXhujANcH8cQ54w130_provenance.
- NP768965.RA3xX33O34SrYR3V7IV6cnwpjkVtfNcXhujANcH8cQ54w130_assertion description "[Mutations in the valosin-containing protein (VCP) gene were recently reported to be the cause of 1%-2% of familial amyotrophic lateral sclerosis (ALS) cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768965.RA3xX33O34SrYR3V7IV6cnwpjkVtfNcXhujANcH8cQ54w130_provenance.
- NP768965.RA3xX33O34SrYR3V7IV6cnwpjkVtfNcXhujANcH8cQ54w130_assertion evidence source_evidence_literature NP768965.RA3xX33O34SrYR3V7IV6cnwpjkVtfNcXhujANcH8cQ54w130_provenance.
- NP768965.RA3xX33O34SrYR3V7IV6cnwpjkVtfNcXhujANcH8cQ54w130_assertion SIO_000772 22078486 NP768965.RA3xX33O34SrYR3V7IV6cnwpjkVtfNcXhujANcH8cQ54w130_provenance.
- NP768965.RA3xX33O34SrYR3V7IV6cnwpjkVtfNcXhujANcH8cQ54w130_assertion wasDerivedFrom befree-20150227 NP768965.RA3xX33O34SrYR3V7IV6cnwpjkVtfNcXhujANcH8cQ54w130_provenance.
- NP768965.RA3xX33O34SrYR3V7IV6cnwpjkVtfNcXhujANcH8cQ54w130_assertion wasGeneratedBy ECO_0000203 NP768965.RA3xX33O34SrYR3V7IV6cnwpjkVtfNcXhujANcH8cQ54w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP768965.RA3xX33O34SrYR3V7IV6cnwpjkVtfNcXhujANcH8cQ54w130_provenance.