Matches in Nanopublications for { ?s ?p "[In summary, we conclude that genetic variations in UBQLN2 and PFN1 in a predominantly Flanders-Belgian cohort of FTLD and ALS patients are extremely rare.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP260935.RAkWtRBclIXiK9aXBW89fydYESU_-cND14HCt6jgCVNj4130_assertion description "[In summary, we conclude that genetic variations in UBQLN2 and PFN1 in a predominantly Flanders-Belgian cohort of FTLD and ALS patients are extremely rare.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP260935.RAkWtRBclIXiK9aXBW89fydYESU_-cND14HCt6jgCVNj4130_provenance.
- NP188928.RAgLHC_VAJ95dLbTuM8g-0_8fwjLiMkKhnw6vr1WpSw9Q130_assertion description "[In summary, we conclude that genetic variations in UBQLN2 and PFN1 in a predominantly Flanders-Belgian cohort of FTLD and ALS patients are extremely rare.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188928.RAgLHC_VAJ95dLbTuM8g-0_8fwjLiMkKhnw6vr1WpSw9Q130_provenance.
- NP657566.RAmHl2IOU69qk9JbZ4MGCK_fve-fWKtfRFwVg8pVgFxm0130_assertion description "[In summary, we conclude that genetic variations in UBQLN2 and PFN1 in a predominantly Flanders-Belgian cohort of FTLD and ALS patients are extremely rare.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP657566.RAmHl2IOU69qk9JbZ4MGCK_fve-fWKtfRFwVg8pVgFxm0130_provenance.
- NP800180.RAibqInW-OVY4B4A7UxJXABFqha89DaS564BYi6py-gmo130_assertion description "[In summary, we conclude that genetic variations in UBQLN2 and PFN1 in a predominantly Flanders-Belgian cohort of FTLD and ALS patients are extremely rare.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP800180.RAibqInW-OVY4B4A7UxJXABFqha89DaS564BYi6py-gmo130_provenance.
- NP640241.RAaeCEHsUgXDD0J1qO2I3kR_Fy80CNsVy0TnNG0YjH2DI130_assertion description "[In summary, we conclude that genetic variations in UBQLN2 and PFN1 in a predominantly Flanders-Belgian cohort of FTLD and ALS patients are extremely rare.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP640241.RAaeCEHsUgXDD0J1qO2I3kR_Fy80CNsVy0TnNG0YjH2DI130_provenance.
- assertion description "[In summary, we conclude that genetic variations in UBQLN2 and PFN1 in a predominantly Flanders-Belgian cohort of FTLD and ALS patients are extremely rare.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[In summary, we conclude that genetic variations in UBQLN2 and PFN1 in a predominantly Flanders-Belgian cohort of FTLD and ALS patients are extremely rare.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1042988.RAd3shWUJx7Tn9biw2sFnj0-byFUU1rkjaB94mf4Tmaxg130_assertion description "[In summary, we conclude that genetic variations in UBQLN2 and PFN1 in a predominantly Flanders-Belgian cohort of FTLD and ALS patients are extremely rare.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1042988.RAd3shWUJx7Tn9biw2sFnj0-byFUU1rkjaB94mf4Tmaxg130_provenance.
- NP1042983.RAuB82KOhkQs8RyswEvZ_ZO8zUBteayEOSIoHgjqjOFL8130_assertion description "[In summary, we conclude that genetic variations in UBQLN2 and PFN1 in a predominantly Flanders-Belgian cohort of FTLD and ALS patients are extremely rare.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1042983.RAuB82KOhkQs8RyswEvZ_ZO8zUBteayEOSIoHgjqjOFL8130_provenance.
- NP616720.RA_oDAfR0icnfQM-Lump0wTLzuyjQgU_8RgoeIhQwfsk0130_assertion description "[In summary, we conclude that genetic variations in UBQLN2 and PFN1 in a predominantly Flanders-Belgian cohort of FTLD and ALS patients are extremely rare.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616720.RA_oDAfR0icnfQM-Lump0wTLzuyjQgU_8RgoeIhQwfsk0130_provenance.