Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP623090.RAPP3pI9beTjuN_pmNeo5bG-AXWknhxxkCtgM8k22tV3M130_assertion> ?p ?o ?g. }
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- NP623090.RAPP3pI9beTjuN_pmNeo5bG-AXWknhxxkCtgM8k22tV3M130_assertion type Assertion NP623090.RAPP3pI9beTjuN_pmNeo5bG-AXWknhxxkCtgM8k22tV3M130_head.
- NP623090.RAPP3pI9beTjuN_pmNeo5bG-AXWknhxxkCtgM8k22tV3M130_assertion description "[Batten disease (juvenile neuronal ceroid lipofuscinosis, JNCL), the most common neurodegenerative disease of childhood, is caused by mutations in the CLN3 gene encoding a putative transmembrane protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623090.RAPP3pI9beTjuN_pmNeo5bG-AXWknhxxkCtgM8k22tV3M130_provenance.
- NP623090.RAPP3pI9beTjuN_pmNeo5bG-AXWknhxxkCtgM8k22tV3M130_assertion evidence source_evidence_literature NP623090.RAPP3pI9beTjuN_pmNeo5bG-AXWknhxxkCtgM8k22tV3M130_provenance.
- NP623090.RAPP3pI9beTjuN_pmNeo5bG-AXWknhxxkCtgM8k22tV3M130_assertion SIO_000772 11590129 NP623090.RAPP3pI9beTjuN_pmNeo5bG-AXWknhxxkCtgM8k22tV3M130_provenance.
- NP623090.RAPP3pI9beTjuN_pmNeo5bG-AXWknhxxkCtgM8k22tV3M130_assertion wasDerivedFrom befree-20140225 NP623090.RAPP3pI9beTjuN_pmNeo5bG-AXWknhxxkCtgM8k22tV3M130_provenance.
- NP623090.RAPP3pI9beTjuN_pmNeo5bG-AXWknhxxkCtgM8k22tV3M130_assertion wasGeneratedBy ECO_0000203 NP623090.RAPP3pI9beTjuN_pmNeo5bG-AXWknhxxkCtgM8k22tV3M130_provenance.