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- source_evidence_literature type ECO_0000212 NP1151070.RAn-mRE7TGKSQYKLeLqMNdrbEUb7UiVoudhb1pj8NR_BA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1151070.RAn-mRE7TGKSQYKLeLqMNdrbEUb7UiVoudhb1pj8NR_BA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1151070.RAn-mRE7TGKSQYKLeLqMNdrbEUb7UiVoudhb1pj8NR_BA130_provenance.
- NP1151070.RAn-mRE7TGKSQYKLeLqMNdrbEUb7UiVoudhb1pj8NR_BA130_assertion description "[Recently SQSTM1 mutations have also been reported in a small number of patients with amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD), neurodegenerative disorders in which significant coexistence with PDB has not been previously recognized.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1151070.RAn-mRE7TGKSQYKLeLqMNdrbEUb7UiVoudhb1pj8NR_BA130_provenance.
- NP1151070.RAn-mRE7TGKSQYKLeLqMNdrbEUb7UiVoudhb1pj8NR_BA130_assertion evidence source_evidence_literature NP1151070.RAn-mRE7TGKSQYKLeLqMNdrbEUb7UiVoudhb1pj8NR_BA130_provenance.
- NP1151070.RAn-mRE7TGKSQYKLeLqMNdrbEUb7UiVoudhb1pj8NR_BA130_assertion SIO_000772 24486447 NP1151070.RAn-mRE7TGKSQYKLeLqMNdrbEUb7UiVoudhb1pj8NR_BA130_provenance.
- NP1151070.RAn-mRE7TGKSQYKLeLqMNdrbEUb7UiVoudhb1pj8NR_BA130_assertion wasDerivedFrom befree-2016 NP1151070.RAn-mRE7TGKSQYKLeLqMNdrbEUb7UiVoudhb1pj8NR_BA130_provenance.
- NP1151070.RAn-mRE7TGKSQYKLeLqMNdrbEUb7UiVoudhb1pj8NR_BA130_assertion wasGeneratedBy ECO_0000203 NP1151070.RAn-mRE7TGKSQYKLeLqMNdrbEUb7UiVoudhb1pj8NR_BA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1151070.RAn-mRE7TGKSQYKLeLqMNdrbEUb7UiVoudhb1pj8NR_BA130_provenance.