Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP413217.RAnftOzI8zg8TVGOp_CKOFth5_1pswtijJkE9LrJeQSKA130_assertion> ?p ?o ?g. }
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- NP413217.RAnftOzI8zg8TVGOp_CKOFth5_1pswtijJkE9LrJeQSKA130_assertion type Assertion NP413217.RAnftOzI8zg8TVGOp_CKOFth5_1pswtijJkE9LrJeQSKA130_head.
- NP413217.RAnftOzI8zg8TVGOp_CKOFth5_1pswtijJkE9LrJeQSKA130_assertion description "[More recently, progranulin gene mutations were recognized in association with the familial form of FTLD and a hexanucleotide repetition in C9ORF72 has been shown to be responsible for familial FTLD and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP413217.RAnftOzI8zg8TVGOp_CKOFth5_1pswtijJkE9LrJeQSKA130_provenance.
- NP413217.RAnftOzI8zg8TVGOp_CKOFth5_1pswtijJkE9LrJeQSKA130_assertion evidence source_evidence_literature NP413217.RAnftOzI8zg8TVGOp_CKOFth5_1pswtijJkE9LrJeQSKA130_provenance.
- NP413217.RAnftOzI8zg8TVGOp_CKOFth5_1pswtijJkE9LrJeQSKA130_assertion SIO_000772 22532172 NP413217.RAnftOzI8zg8TVGOp_CKOFth5_1pswtijJkE9LrJeQSKA130_provenance.
- NP413217.RAnftOzI8zg8TVGOp_CKOFth5_1pswtijJkE9LrJeQSKA130_assertion wasDerivedFrom befree-20140225 NP413217.RAnftOzI8zg8TVGOp_CKOFth5_1pswtijJkE9LrJeQSKA130_provenance.
- NP413217.RAnftOzI8zg8TVGOp_CKOFth5_1pswtijJkE9LrJeQSKA130_assertion wasGeneratedBy ECO_0000203 NP413217.RAnftOzI8zg8TVGOp_CKOFth5_1pswtijJkE9LrJeQSKA130_provenance.