Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1215478.RAFFVo9arP3Xba831c7LsD2BT5Mpz7v7XV9_Qr08_DZGE130_assertion> ?p ?o ?g. }
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- NP1215478.RAFFVo9arP3Xba831c7LsD2BT5Mpz7v7XV9_Qr08_DZGE130_assertion type Assertion NP1215478.RAFFVo9arP3Xba831c7LsD2BT5Mpz7v7XV9_Qr08_DZGE130_head.
- NP1215478.RAFFVo9arP3Xba831c7LsD2BT5Mpz7v7XV9_Qr08_DZGE130_assertion description "[In total, we identified 78 potentially damaging rare variants (frequency <1%), including ABCA7 p.L400V in a family with Alzheimer's disease and LRRK2 p.R1514Q in 6 of 98 patients with Parkinson's disease (6.1%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1215478.RAFFVo9arP3Xba831c7LsD2BT5Mpz7v7XV9_Qr08_DZGE130_provenance.
- NP1215478.RAFFVo9arP3Xba831c7LsD2BT5Mpz7v7XV9_Qr08_DZGE130_assertion evidence source_evidence_literature NP1215478.RAFFVo9arP3Xba831c7LsD2BT5Mpz7v7XV9_Qr08_DZGE130_provenance.
- NP1215478.RAFFVo9arP3Xba831c7LsD2BT5Mpz7v7XV9_Qr08_DZGE130_assertion SIO_000772 25174650 NP1215478.RAFFVo9arP3Xba831c7LsD2BT5Mpz7v7XV9_Qr08_DZGE130_provenance.
- NP1215478.RAFFVo9arP3Xba831c7LsD2BT5Mpz7v7XV9_Qr08_DZGE130_assertion wasDerivedFrom befree-2016 NP1215478.RAFFVo9arP3Xba831c7LsD2BT5Mpz7v7XV9_Qr08_DZGE130_provenance.
- NP1215478.RAFFVo9arP3Xba831c7LsD2BT5Mpz7v7XV9_Qr08_DZGE130_assertion wasGeneratedBy ECO_0000203 NP1215478.RAFFVo9arP3Xba831c7LsD2BT5Mpz7v7XV9_Qr08_DZGE130_provenance.