Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP210855.RA9CEga7JYfLTVjNfbNSJQ1683xcVHxSDT_8pMtk39y94130_assertion> ?p ?o ?g. }
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- NP210855.RA9CEga7JYfLTVjNfbNSJQ1683xcVHxSDT_8pMtk39y94130_assertion type Assertion NP210855.RA9CEga7JYfLTVjNfbNSJQ1683xcVHxSDT_8pMtk39y94130_head.
- NP210855.RA9CEga7JYfLTVjNfbNSJQ1683xcVHxSDT_8pMtk39y94130_assertion description "[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." NP210855.RA9CEga7JYfLTVjNfbNSJQ1683xcVHxSDT_8pMtk39y94130_provenance.
- NP210855.RA9CEga7JYfLTVjNfbNSJQ1683xcVHxSDT_8pMtk39y94130_assertion evidence source_evidence_literature NP210855.RA9CEga7JYfLTVjNfbNSJQ1683xcVHxSDT_8pMtk39y94130_provenance.
- NP210855.RA9CEga7JYfLTVjNfbNSJQ1683xcVHxSDT_8pMtk39y94130_assertion SIO_000772 20412296 NP210855.RA9CEga7JYfLTVjNfbNSJQ1683xcVHxSDT_8pMtk39y94130_provenance.
- NP210855.RA9CEga7JYfLTVjNfbNSJQ1683xcVHxSDT_8pMtk39y94130_assertion wasDerivedFrom befree-20140225 NP210855.RA9CEga7JYfLTVjNfbNSJQ1683xcVHxSDT_8pMtk39y94130_provenance.
- NP210855.RA9CEga7JYfLTVjNfbNSJQ1683xcVHxSDT_8pMtk39y94130_assertion wasGeneratedBy ECO_0000203 NP210855.RA9CEga7JYfLTVjNfbNSJQ1683xcVHxSDT_8pMtk39y94130_provenance.