Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP316053.RATopEr6pfRFOp8_9M2OCiT58FOL7Mc0Lt_-MwK7GoXYg130_assertion> ?p ?o ?g. }
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- NP316053.RATopEr6pfRFOp8_9M2OCiT58FOL7Mc0Lt_-MwK7GoXYg130_assertion type Assertion NP316053.RATopEr6pfRFOp8_9M2OCiT58FOL7Mc0Lt_-MwK7GoXYg130_head.
- 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.