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- source_evidence_literature type ECO_0000212 NP919523.RAcq5spwLfWu-UhuH_WMrGbLwTTY5WBD75FVCzyauLF88130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP919523.RAcq5spwLfWu-UhuH_WMrGbLwTTY5WBD75FVCzyauLF88130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP919523.RAcq5spwLfWu-UhuH_WMrGbLwTTY5WBD75FVCzyauLF88130_provenance.
- NP919523.RAcq5spwLfWu-UhuH_WMrGbLwTTY5WBD75FVCzyauLF88130_assertion description "[The secondary ?-dystroglycanopathies usually present in infancy as congenital muscular dystrophies but may manifest later in childhood or adult life (limb-girdle muscular dystrophy (LGMD) 2I, LGMD2K, LGMD2M, LGMD2N, and LGMD2O).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919523.RAcq5spwLfWu-UhuH_WMrGbLwTTY5WBD75FVCzyauLF88130_provenance.
- NP919523.RAcq5spwLfWu-UhuH_WMrGbLwTTY5WBD75FVCzyauLF88130_assertion evidence source_evidence_literature NP919523.RAcq5spwLfWu-UhuH_WMrGbLwTTY5WBD75FVCzyauLF88130_provenance.
- NP919523.RAcq5spwLfWu-UhuH_WMrGbLwTTY5WBD75FVCzyauLF88130_assertion SIO_000772 21496628 NP919523.RAcq5spwLfWu-UhuH_WMrGbLwTTY5WBD75FVCzyauLF88130_provenance.
- NP919523.RAcq5spwLfWu-UhuH_WMrGbLwTTY5WBD75FVCzyauLF88130_assertion wasDerivedFrom befree-20150227 NP919523.RAcq5spwLfWu-UhuH_WMrGbLwTTY5WBD75FVCzyauLF88130_provenance.
- NP919523.RAcq5spwLfWu-UhuH_WMrGbLwTTY5WBD75FVCzyauLF88130_assertion wasGeneratedBy ECO_0000203 NP919523.RAcq5spwLfWu-UhuH_WMrGbLwTTY5WBD75FVCzyauLF88130_provenance.
- befree-20150227 importedOn "2015-02-27" NP919523.RAcq5spwLfWu-UhuH_WMrGbLwTTY5WBD75FVCzyauLF88130_provenance.