Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP316051.RAKKn7rCv9Q1hWdmUALFdUN8tbJC92T4YCa2g_L1bf5V8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP316051.RAKKn7rCv9Q1hWdmUALFdUN8tbJC92T4YCa2g_L1bf5V8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP316051.RAKKn7rCv9Q1hWdmUALFdUN8tbJC92T4YCa2g_L1bf5V8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP316051.RAKKn7rCv9Q1hWdmUALFdUN8tbJC92T4YCa2g_L1bf5V8130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP316051.RAKKn7rCv9Q1hWdmUALFdUN8tbJC92T4YCa2g_L1bf5V8130_provenance.