Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP700664.RA89FdKtCWxo2w7b-zNFerbWHDCJjOLLkmMchqUhnexcQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP700664.RA89FdKtCWxo2w7b-zNFerbWHDCJjOLLkmMchqUhnexcQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP700664.RA89FdKtCWxo2w7b-zNFerbWHDCJjOLLkmMchqUhnexcQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP700664.RA89FdKtCWxo2w7b-zNFerbWHDCJjOLLkmMchqUhnexcQ130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP700664.RA89FdKtCWxo2w7b-zNFerbWHDCJjOLLkmMchqUhnexcQ130_provenance.