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- NP900099.RAZLADRVH5lD0KDhnBEmnfQQ8PnVLJHNGghwoUiNMVO64130_assertion type Assertion NP900099.RAZLADRVH5lD0KDhnBEmnfQQ8PnVLJHNGghwoUiNMVO64130_head.
- NP900099.RAZLADRVH5lD0KDhnBEmnfQQ8PnVLJHNGghwoUiNMVO64130_assertion wasGeneratedBy ECO_0000203 NP900099.RAZLADRVH5lD0KDhnBEmnfQQ8PnVLJHNGghwoUiNMVO64130_provenance.
- NP900099.RAZLADRVH5lD0KDhnBEmnfQQ8PnVLJHNGghwoUiNMVO64130_assertion wasDerivedFrom befree-20140225 NP900099.RAZLADRVH5lD0KDhnBEmnfQQ8PnVLJHNGghwoUiNMVO64130_provenance.
- NP900099.RAZLADRVH5lD0KDhnBEmnfQQ8PnVLJHNGghwoUiNMVO64130_assertion SIO_000772 11749051 NP900099.RAZLADRVH5lD0KDhnBEmnfQQ8PnVLJHNGghwoUiNMVO64130_provenance.
- NP900099.RAZLADRVH5lD0KDhnBEmnfQQ8PnVLJHNGghwoUiNMVO64130_assertion evidence source_evidence_literature NP900099.RAZLADRVH5lD0KDhnBEmnfQQ8PnVLJHNGghwoUiNMVO64130_provenance.
- NP900099.RAZLADRVH5lD0KDhnBEmnfQQ8PnVLJHNGghwoUiNMVO64130_assertion description "[Hence, autosomal dominant inclusion body myopathy (HIBM), Paget disease of bone (PDB), and frontotemporal dementia (FTD) localizes to a 1.08-6.46 cM critical interval on 9p13.3-12 in the region of autosomal recessive IBM2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP900099.RAZLADRVH5lD0KDhnBEmnfQQ8PnVLJHNGghwoUiNMVO64130_provenance.