Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP700664.RA89FdKtCWxo2w7b-zNFerbWHDCJjOLLkmMchqUhnexcQ130_assertion> ?p ?o ?g. }
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- NP700664.RA89FdKtCWxo2w7b-zNFerbWHDCJjOLLkmMchqUhnexcQ130_assertion type Assertion NP700664.RA89FdKtCWxo2w7b-zNFerbWHDCJjOLLkmMchqUhnexcQ130_head.
- NP700664.RA89FdKtCWxo2w7b-zNFerbWHDCJjOLLkmMchqUhnexcQ130_assertion description "[Sensenbrenner syndrome/cranioectodermal dysplasia (CED) is an autosomal-recessive disease that is characterized by craniosynostosis and ectodermal and skeletal abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP700664.RA89FdKtCWxo2w7b-zNFerbWHDCJjOLLkmMchqUhnexcQ130_provenance.
- NP700664.RA89FdKtCWxo2w7b-zNFerbWHDCJjOLLkmMchqUhnexcQ130_assertion evidence source_evidence_literature NP700664.RA89FdKtCWxo2w7b-zNFerbWHDCJjOLLkmMchqUhnexcQ130_provenance.
- NP700664.RA89FdKtCWxo2w7b-zNFerbWHDCJjOLLkmMchqUhnexcQ130_assertion SIO_000772 20817137 NP700664.RA89FdKtCWxo2w7b-zNFerbWHDCJjOLLkmMchqUhnexcQ130_provenance.
- NP700664.RA89FdKtCWxo2w7b-zNFerbWHDCJjOLLkmMchqUhnexcQ130_assertion wasDerivedFrom befree-20140225 NP700664.RA89FdKtCWxo2w7b-zNFerbWHDCJjOLLkmMchqUhnexcQ130_provenance.
- NP700664.RA89FdKtCWxo2w7b-zNFerbWHDCJjOLLkmMchqUhnexcQ130_assertion wasGeneratedBy ECO_0000203 NP700664.RA89FdKtCWxo2w7b-zNFerbWHDCJjOLLkmMchqUhnexcQ130_provenance.