Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP775529.RAAKuPoZRYYuWb9LtSAgA-BezxzojC1R4X48bMiCA94aM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP775529.RAAKuPoZRYYuWb9LtSAgA-BezxzojC1R4X48bMiCA94aM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP775529.RAAKuPoZRYYuWb9LtSAgA-BezxzojC1R4X48bMiCA94aM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP775529.RAAKuPoZRYYuWb9LtSAgA-BezxzojC1R4X48bMiCA94aM130_provenance.
- NP775529.RAAKuPoZRYYuWb9LtSAgA-BezxzojC1R4X48bMiCA94aM130_assertion description "[Mutations in tripeptidyl-peptidase I (TPP I) underlie the classic late-infantile form of neuronal ceroid lipofuscinoses (CLN2), the most common neurodegenerative disorders of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775529.RAAKuPoZRYYuWb9LtSAgA-BezxzojC1R4X48bMiCA94aM130_provenance.
- NP775529.RAAKuPoZRYYuWb9LtSAgA-BezxzojC1R4X48bMiCA94aM130_assertion evidence source_evidence_literature NP775529.RAAKuPoZRYYuWb9LtSAgA-BezxzojC1R4X48bMiCA94aM130_provenance.
- NP775529.RAAKuPoZRYYuWb9LtSAgA-BezxzojC1R4X48bMiCA94aM130_assertion SIO_000772 16895480 NP775529.RAAKuPoZRYYuWb9LtSAgA-BezxzojC1R4X48bMiCA94aM130_provenance.
- NP775529.RAAKuPoZRYYuWb9LtSAgA-BezxzojC1R4X48bMiCA94aM130_assertion wasDerivedFrom befree-20140225 NP775529.RAAKuPoZRYYuWb9LtSAgA-BezxzojC1R4X48bMiCA94aM130_provenance.
- NP775529.RAAKuPoZRYYuWb9LtSAgA-BezxzojC1R4X48bMiCA94aM130_assertion wasGeneratedBy ECO_0000203 NP775529.RAAKuPoZRYYuWb9LtSAgA-BezxzojC1R4X48bMiCA94aM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP775529.RAAKuPoZRYYuWb9LtSAgA-BezxzojC1R4X48bMiCA94aM130_provenance.