Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1107208.RAK2uFBRavYyaBt6ZiP-UAOdElsA4zb5tNZ_Svb5lVYW8130_assertion> ?p ?o ?g. }
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- NP1107208.RAK2uFBRavYyaBt6ZiP-UAOdElsA4zb5tNZ_Svb5lVYW8130_assertion type Assertion NP1107208.RAK2uFBRavYyaBt6ZiP-UAOdElsA4zb5tNZ_Svb5lVYW8130_head.
- NP1107208.RAK2uFBRavYyaBt6ZiP-UAOdElsA4zb5tNZ_Svb5lVYW8130_assertion description "[We developed gene panel based technologies to assess 16 genes known to harbour mutations causal of dementia and combined these with PCR based assessments of the C9orf72 hexanucleotide repeat expansion and the octapeptide repeat region of PRNP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1107208.RAK2uFBRavYyaBt6ZiP-UAOdElsA4zb5tNZ_Svb5lVYW8130_provenance.
- NP1107208.RAK2uFBRavYyaBt6ZiP-UAOdElsA4zb5tNZ_Svb5lVYW8130_assertion evidence source_evidence_literature NP1107208.RAK2uFBRavYyaBt6ZiP-UAOdElsA4zb5tNZ_Svb5lVYW8130_provenance.
- NP1107208.RAK2uFBRavYyaBt6ZiP-UAOdElsA4zb5tNZ_Svb5lVYW8130_assertion SIO_000772 23998997 NP1107208.RAK2uFBRavYyaBt6ZiP-UAOdElsA4zb5tNZ_Svb5lVYW8130_provenance.
- NP1107208.RAK2uFBRavYyaBt6ZiP-UAOdElsA4zb5tNZ_Svb5lVYW8130_assertion wasDerivedFrom befree-2016 NP1107208.RAK2uFBRavYyaBt6ZiP-UAOdElsA4zb5tNZ_Svb5lVYW8130_provenance.
- NP1107208.RAK2uFBRavYyaBt6ZiP-UAOdElsA4zb5tNZ_Svb5lVYW8130_assertion wasGeneratedBy ECO_0000203 NP1107208.RAK2uFBRavYyaBt6ZiP-UAOdElsA4zb5tNZ_Svb5lVYW8130_provenance.