Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP316051.RAKKn7rCv9Q1hWdmUALFdUN8tbJC92T4YCa2g_L1bf5V8130_assertion> ?p ?o ?g. }
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- NP316051.RAKKn7rCv9Q1hWdmUALFdUN8tbJC92T4YCa2g_L1bf5V8130_assertion type Assertion NP316051.RAKKn7rCv9Q1hWdmUALFdUN8tbJC92T4YCa2g_L1bf5V8130_head.
- NP316051.RAKKn7rCv9Q1hWdmUALFdUN8tbJC92T4YCa2g_L1bf5V8130_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." NP316051.RAKKn7rCv9Q1hWdmUALFdUN8tbJC92T4YCa2g_L1bf5V8130_provenance.
- NP316051.RAKKn7rCv9Q1hWdmUALFdUN8tbJC92T4YCa2g_L1bf5V8130_assertion evidence source_evidence_literature NP316051.RAKKn7rCv9Q1hWdmUALFdUN8tbJC92T4YCa2g_L1bf5V8130_provenance.
- NP316051.RAKKn7rCv9Q1hWdmUALFdUN8tbJC92T4YCa2g_L1bf5V8130_assertion SIO_000772 16895480 NP316051.RAKKn7rCv9Q1hWdmUALFdUN8tbJC92T4YCa2g_L1bf5V8130_provenance.
- NP316051.RAKKn7rCv9Q1hWdmUALFdUN8tbJC92T4YCa2g_L1bf5V8130_assertion wasDerivedFrom befree-20150227 NP316051.RAKKn7rCv9Q1hWdmUALFdUN8tbJC92T4YCa2g_L1bf5V8130_provenance.
- NP316051.RAKKn7rCv9Q1hWdmUALFdUN8tbJC92T4YCa2g_L1bf5V8130_assertion wasGeneratedBy ECO_0000203 NP316051.RAKKn7rCv9Q1hWdmUALFdUN8tbJC92T4YCa2g_L1bf5V8130_provenance.