Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP316053.RATopEr6pfRFOp8_9M2OCiT58FOL7Mc0Lt_-MwK7GoXYg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP316053.RATopEr6pfRFOp8_9M2OCiT58FOL7Mc0Lt_-MwK7GoXYg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP316053.RATopEr6pfRFOp8_9M2OCiT58FOL7Mc0Lt_-MwK7GoXYg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP316053.RATopEr6pfRFOp8_9M2OCiT58FOL7Mc0Lt_-MwK7GoXYg130_provenance.
- NP316053.RATopEr6pfRFOp8_9M2OCiT58FOL7Mc0Lt_-MwK7GoXYg130_assertion description "[Tripeptidyl peptidase 1 (TPP1) deficiency causes CLN2 disease, late infantile (or classic late infantile neuronal ceroid lipofuscinosis), a paediatric neurodegenerative disease of autosomal recessive inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316053.RATopEr6pfRFOp8_9M2OCiT58FOL7Mc0Lt_-MwK7GoXYg130_provenance.
- NP316053.RATopEr6pfRFOp8_9M2OCiT58FOL7Mc0Lt_-MwK7GoXYg130_assertion evidence source_evidence_literature NP316053.RATopEr6pfRFOp8_9M2OCiT58FOL7Mc0Lt_-MwK7GoXYg130_provenance.
- NP316053.RATopEr6pfRFOp8_9M2OCiT58FOL7Mc0Lt_-MwK7GoXYg130_assertion SIO_000772 23587805 NP316053.RATopEr6pfRFOp8_9M2OCiT58FOL7Mc0Lt_-MwK7GoXYg130_provenance.
- NP316053.RATopEr6pfRFOp8_9M2OCiT58FOL7Mc0Lt_-MwK7GoXYg130_assertion wasDerivedFrom befree-20150227 NP316053.RATopEr6pfRFOp8_9M2OCiT58FOL7Mc0Lt_-MwK7GoXYg130_provenance.
- NP316053.RATopEr6pfRFOp8_9M2OCiT58FOL7Mc0Lt_-MwK7GoXYg130_assertion wasGeneratedBy ECO_0000203 NP316053.RATopEr6pfRFOp8_9M2OCiT58FOL7Mc0Lt_-MwK7GoXYg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP316053.RATopEr6pfRFOp8_9M2OCiT58FOL7Mc0Lt_-MwK7GoXYg130_provenance.