Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP722363.RARS797q21Mx5jMQixNd_ILvSmt2UYVkEs0kfNPtOACu4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP722363.RARS797q21Mx5jMQixNd_ILvSmt2UYVkEs0kfNPtOACu4130_assertion type Assertion NP722363.RARS797q21Mx5jMQixNd_ILvSmt2UYVkEs0kfNPtOACu4130_head.
- NP722363.RARS797q21Mx5jMQixNd_ILvSmt2UYVkEs0kfNPtOACu4130_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." NP722363.RARS797q21Mx5jMQixNd_ILvSmt2UYVkEs0kfNPtOACu4130_provenance.
- NP722363.RARS797q21Mx5jMQixNd_ILvSmt2UYVkEs0kfNPtOACu4130_assertion evidence source_evidence_literature NP722363.RARS797q21Mx5jMQixNd_ILvSmt2UYVkEs0kfNPtOACu4130_provenance.
- NP722363.RARS797q21Mx5jMQixNd_ILvSmt2UYVkEs0kfNPtOACu4130_assertion SIO_000772 11590129 NP722363.RARS797q21Mx5jMQixNd_ILvSmt2UYVkEs0kfNPtOACu4130_provenance.
- NP722363.RARS797q21Mx5jMQixNd_ILvSmt2UYVkEs0kfNPtOACu4130_assertion wasDerivedFrom befree-20140225 NP722363.RARS797q21Mx5jMQixNd_ILvSmt2UYVkEs0kfNPtOACu4130_provenance.
- NP722363.RARS797q21Mx5jMQixNd_ILvSmt2UYVkEs0kfNPtOACu4130_assertion wasGeneratedBy ECO_0000203 NP722363.RARS797q21Mx5jMQixNd_ILvSmt2UYVkEs0kfNPtOACu4130_provenance.