Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP968271.RA48-CuP1KhEMHu9WhWkDgrb3B3nYZOt7LkMrIGwzv2bM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP968271.RA48-CuP1KhEMHu9WhWkDgrb3B3nYZOt7LkMrIGwzv2bM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP968271.RA48-CuP1KhEMHu9WhWkDgrb3B3nYZOt7LkMrIGwzv2bM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP968271.RA48-CuP1KhEMHu9WhWkDgrb3B3nYZOt7LkMrIGwzv2bM130_provenance.
- NP968271.RA48-CuP1KhEMHu9WhWkDgrb3B3nYZOt7LkMrIGwzv2bM130_assertion description "[Spinocerebellar ataxia with axonal neuropathy-1 (SCAN1) is a neurodegenerative disease that results from mutation of tyrosyl phosphodiesterase 1 (TDP1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP968271.RA48-CuP1KhEMHu9WhWkDgrb3B3nYZOt7LkMrIGwzv2bM130_provenance.
- NP968271.RA48-CuP1KhEMHu9WhWkDgrb3B3nYZOt7LkMrIGwzv2bM130_assertion evidence source_evidence_literature NP968271.RA48-CuP1KhEMHu9WhWkDgrb3B3nYZOt7LkMrIGwzv2bM130_provenance.
- NP968271.RA48-CuP1KhEMHu9WhWkDgrb3B3nYZOt7LkMrIGwzv2bM130_assertion SIO_000772 15744309 NP968271.RA48-CuP1KhEMHu9WhWkDgrb3B3nYZOt7LkMrIGwzv2bM130_provenance.
- NP968271.RA48-CuP1KhEMHu9WhWkDgrb3B3nYZOt7LkMrIGwzv2bM130_assertion wasDerivedFrom befree-20150227 NP968271.RA48-CuP1KhEMHu9WhWkDgrb3B3nYZOt7LkMrIGwzv2bM130_provenance.
- NP968271.RA48-CuP1KhEMHu9WhWkDgrb3B3nYZOt7LkMrIGwzv2bM130_assertion wasGeneratedBy ECO_0000203 NP968271.RA48-CuP1KhEMHu9WhWkDgrb3B3nYZOt7LkMrIGwzv2bM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP968271.RA48-CuP1KhEMHu9WhWkDgrb3B3nYZOt7LkMrIGwzv2bM130_provenance.