Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP959193.RAQ1oC3T0YXtbWgoPxhjpu3WaW7TADf1ZK478CSHM23Dg130_assertion> ?p ?o ?g. }
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- NP959193.RAQ1oC3T0YXtbWgoPxhjpu3WaW7TADf1ZK478CSHM23Dg130_assertion type Assertion NP959193.RAQ1oC3T0YXtbWgoPxhjpu3WaW7TADf1ZK478CSHM23Dg130_head.
- NP959193.RAQ1oC3T0YXtbWgoPxhjpu3WaW7TADf1ZK478CSHM23Dg130_assertion description "[Pathogenic mutations in APP, PSEN1, PSEN2, MAPT and GRN have previously been linked to familial early onset forms of dementia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP959193.RAQ1oC3T0YXtbWgoPxhjpu3WaW7TADf1ZK478CSHM23Dg130_provenance.
- NP959193.RAQ1oC3T0YXtbWgoPxhjpu3WaW7TADf1ZK478CSHM23Dg130_assertion evidence source_evidence_literature NP959193.RAQ1oC3T0YXtbWgoPxhjpu3WaW7TADf1ZK478CSHM23Dg130_provenance.
- NP959193.RAQ1oC3T0YXtbWgoPxhjpu3WaW7TADf1ZK478CSHM23Dg130_assertion SIO_000772 22312439 NP959193.RAQ1oC3T0YXtbWgoPxhjpu3WaW7TADf1ZK478CSHM23Dg130_provenance.
- NP959193.RAQ1oC3T0YXtbWgoPxhjpu3WaW7TADf1ZK478CSHM23Dg130_assertion wasDerivedFrom befree-2016 NP959193.RAQ1oC3T0YXtbWgoPxhjpu3WaW7TADf1ZK478CSHM23Dg130_provenance.
- NP959193.RAQ1oC3T0YXtbWgoPxhjpu3WaW7TADf1ZK478CSHM23Dg130_assertion wasGeneratedBy ECO_0000203 NP959193.RAQ1oC3T0YXtbWgoPxhjpu3WaW7TADf1ZK478CSHM23Dg130_provenance.