Showing results (71-80 of 86) with videos related to

Sort By:
Pageof 9
Plant Science : an International Journal of Experimental Plant Biology|December 8, 2020
The TaCslA12 gene expressed in the wheat grain endosperm synthesizes wheat-like mannan when expressed in yeast and ArabidopsisYves Verhertbruggen, Axelle Bouder, Jacqueline Vigouroux, et al.
Journal of Biomedical Semantics|March 8, 2014
The Semanticscience Integrated Ontology (SIO) for biomedical research and knowledge discoveryMichel Dumontier, Christopher Jo Baker, Joachim Baran, et al.
Molecular Genetics and Metabolism|March 14, 2025
SIMPATHIC: Accelerating drug repurposing for rare diseases by exploiting SIMilarities in clinical and molecular PATHologyClara D M van Karnebeek, Annelieke R Müller, Laura Benkemoun, et al.
Journal of Neuromuscular Diseases|October 1, 2025
The FAIR journey of a patient-driven registry: Reflections and practical solutions from the Duchenne Data Platform FAIRification experienceNawel Lalout, Mark D Wilkinson, Dagmar Wandrei, et al.
Orphanet Journal of Rare Diseases|December 14, 2022
Towards FAIRification of sensitive and fragmented rare disease patient data: challenges and solutions in European reference network registriesBruna Dos Santos Vieira, César H Bernabé, Shuxin Zhang, et al.
Genome Research|October 9, 2002
The Bioperl toolkit: Perl modules for the life sciencesJason E Stajich, David Block, Kris Boulez, et al.
Scientific Data|May 8, 2024
Getting your DUCs in a row - standardising the representation of Digital Use ConditionsFrancis Jeanson, Spencer J Gibson, Pinar Alper, et al.
Journal of Biomedical Semantics|March 16, 2022
Semantic modelling of common data elements for rare disease registries, and a prototype workflow for their deployment over registry dataRajaram Kaliyaperumal, Mark D Wilkinson, Pablo Alarcón Moreno, et al.
Scientific Data|May 8, 2024
Common conditions of use elements. Atomic concepts for consistent and effective information governanceMaria Del Carmen Sanchez Gonzalez, Pim Kamerling, Mariapia Iermito, et al.
Orphanet Journal of Rare Diseases|February 14, 2024
EURO-NMD registry: federated FAIR infrastructure, innovative technologies and concepts of a patient-centred registry for rare neuromuscular disordersAntonio Atalaia, Dagmar Wandrei, Nawel Lalout, et al.
Pageof 9