Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP807704.RAIpIEJD0LI4xzb4ES80jI3tgn2X0VKcK8RRyEkVE41ak130_assertion> ?p ?o ?g. }
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- NP807704.RAIpIEJD0LI4xzb4ES80jI3tgn2X0VKcK8RRyEkVE41ak130_assertion type Assertion NP807704.RAIpIEJD0LI4xzb4ES80jI3tgn2X0VKcK8RRyEkVE41ak130_head.
- NP807704.RAIpIEJD0LI4xzb4ES80jI3tgn2X0VKcK8RRyEkVE41ak130_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." NP807704.RAIpIEJD0LI4xzb4ES80jI3tgn2X0VKcK8RRyEkVE41ak130_provenance.
- NP807704.RAIpIEJD0LI4xzb4ES80jI3tgn2X0VKcK8RRyEkVE41ak130_assertion evidence source_evidence_literature NP807704.RAIpIEJD0LI4xzb4ES80jI3tgn2X0VKcK8RRyEkVE41ak130_provenance.
- NP807704.RAIpIEJD0LI4xzb4ES80jI3tgn2X0VKcK8RRyEkVE41ak130_assertion SIO_000772 20412296 NP807704.RAIpIEJD0LI4xzb4ES80jI3tgn2X0VKcK8RRyEkVE41ak130_provenance.
- NP807704.RAIpIEJD0LI4xzb4ES80jI3tgn2X0VKcK8RRyEkVE41ak130_assertion wasDerivedFrom befree-2016 NP807704.RAIpIEJD0LI4xzb4ES80jI3tgn2X0VKcK8RRyEkVE41ak130_provenance.
- NP807704.RAIpIEJD0LI4xzb4ES80jI3tgn2X0VKcK8RRyEkVE41ak130_assertion wasGeneratedBy ECO_0000203 NP807704.RAIpIEJD0LI4xzb4ES80jI3tgn2X0VKcK8RRyEkVE41ak130_provenance.