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- NP587208.RAjqEwccCN5XhPDINpBUap4Or5Nii0qtSDEZJ76Y05xZg130_assertion type Assertion NP587208.RAjqEwccCN5XhPDINpBUap4Or5Nii0qtSDEZJ76Y05xZg130_head.
- NP587208.RAjqEwccCN5XhPDINpBUap4Or5Nii0qtSDEZJ76Y05xZg130_assertion description "[We used homozygosity mapping in two families with autosomal-recessive short-rib polydactyly syndrome Majewski type to identify mutations in NEK1 as an underlying cause of this lethal osteochondrodysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587208.RAjqEwccCN5XhPDINpBUap4Or5Nii0qtSDEZJ76Y05xZg130_provenance.
- NP587208.RAjqEwccCN5XhPDINpBUap4Or5Nii0qtSDEZJ76Y05xZg130_assertion evidence source_evidence_literature NP587208.RAjqEwccCN5XhPDINpBUap4Or5Nii0qtSDEZJ76Y05xZg130_provenance.
- NP587208.RAjqEwccCN5XhPDINpBUap4Or5Nii0qtSDEZJ76Y05xZg130_assertion SIO_000772 21211617 NP587208.RAjqEwccCN5XhPDINpBUap4Or5Nii0qtSDEZJ76Y05xZg130_provenance.
- NP587208.RAjqEwccCN5XhPDINpBUap4Or5Nii0qtSDEZJ76Y05xZg130_assertion wasDerivedFrom befree-20150227 NP587208.RAjqEwccCN5XhPDINpBUap4Or5Nii0qtSDEZJ76Y05xZg130_provenance.
- NP587208.RAjqEwccCN5XhPDINpBUap4Or5Nii0qtSDEZJ76Y05xZg130_assertion wasGeneratedBy ECO_0000203 NP587208.RAjqEwccCN5XhPDINpBUap4Or5Nii0qtSDEZJ76Y05xZg130_provenance.