Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP709302.RA7so5XdNfVoC_KAOCIARoD3M6zPXhLx8-q3SeWOwKzwM130_assertion> ?p ?o ?g. }
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- NP709302.RA7so5XdNfVoC_KAOCIARoD3M6zPXhLx8-q3SeWOwKzwM130_assertion type Assertion NP709302.RA7so5XdNfVoC_KAOCIARoD3M6zPXhLx8-q3SeWOwKzwM130_head.
- NP709302.RA7so5XdNfVoC_KAOCIARoD3M6zPXhLx8-q3SeWOwKzwM130_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." NP709302.RA7so5XdNfVoC_KAOCIARoD3M6zPXhLx8-q3SeWOwKzwM130_provenance.
- NP709302.RA7so5XdNfVoC_KAOCIARoD3M6zPXhLx8-q3SeWOwKzwM130_assertion evidence source_evidence_literature NP709302.RA7so5XdNfVoC_KAOCIARoD3M6zPXhLx8-q3SeWOwKzwM130_provenance.
- NP709302.RA7so5XdNfVoC_KAOCIARoD3M6zPXhLx8-q3SeWOwKzwM130_assertion SIO_000772 20817137 NP709302.RA7so5XdNfVoC_KAOCIARoD3M6zPXhLx8-q3SeWOwKzwM130_provenance.
- NP709302.RA7so5XdNfVoC_KAOCIARoD3M6zPXhLx8-q3SeWOwKzwM130_assertion wasDerivedFrom befree-20140225 NP709302.RA7so5XdNfVoC_KAOCIARoD3M6zPXhLx8-q3SeWOwKzwM130_provenance.
- NP709302.RA7so5XdNfVoC_KAOCIARoD3M6zPXhLx8-q3SeWOwKzwM130_assertion wasGeneratedBy ECO_0000203 NP709302.RA7so5XdNfVoC_KAOCIARoD3M6zPXhLx8-q3SeWOwKzwM130_provenance.