Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP89086.RAi8bUJZd6PpzX1Jk5Iqcoioyha9-HK_FHTG0ns_PHlHg130_assertion> ?p ?o ?g. }
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- NP89086.RAi8bUJZd6PpzX1Jk5Iqcoioyha9-HK_FHTG0ns_PHlHg130_assertion type Assertion NP89086.RAi8bUJZd6PpzX1Jk5Iqcoioyha9-HK_FHTG0ns_PHlHg130_head.
- NP89086.RAi8bUJZd6PpzX1Jk5Iqcoioyha9-HK_FHTG0ns_PHlHg130_assertion description "[Our results confirm that mutations in CHMP2B are not a common cause of FTLD. MAPT and PGRN mutations are also rare in Finnish population, suggesting that other, still unknown genetic factors may play a role in the pathogenesis of FTLD in Finnish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP89086.RAi8bUJZd6PpzX1Jk5Iqcoioyha9-HK_FHTG0ns_PHlHg130_provenance.
- NP89086.RAi8bUJZd6PpzX1Jk5Iqcoioyha9-HK_FHTG0ns_PHlHg130_assertion evidence source_evidence_literature NP89086.RAi8bUJZd6PpzX1Jk5Iqcoioyha9-HK_FHTG0ns_PHlHg130_provenance.
- NP89086.RAi8bUJZd6PpzX1Jk5Iqcoioyha9-HK_FHTG0ns_PHlHg130_assertion SIO_000772 20412296 NP89086.RAi8bUJZd6PpzX1Jk5Iqcoioyha9-HK_FHTG0ns_PHlHg130_provenance.
- NP89086.RAi8bUJZd6PpzX1Jk5Iqcoioyha9-HK_FHTG0ns_PHlHg130_assertion wasDerivedFrom gad-20130706 NP89086.RAi8bUJZd6PpzX1Jk5Iqcoioyha9-HK_FHTG0ns_PHlHg130_provenance.
- NP89086.RAi8bUJZd6PpzX1Jk5Iqcoioyha9-HK_FHTG0ns_PHlHg130_assertion wasGeneratedBy ECO_0000203 NP89086.RAi8bUJZd6PpzX1Jk5Iqcoioyha9-HK_FHTG0ns_PHlHg130_provenance.