Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP331252.RAJPIc0nO1MtXNFyXgUJrJ1ImlE8ysNsVlPswPAuTQOsc130_assertion> ?p ?o ?g. }
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- NP331252.RAJPIc0nO1MtXNFyXgUJrJ1ImlE8ysNsVlPswPAuTQOsc130_assertion type Assertion NP331252.RAJPIc0nO1MtXNFyXgUJrJ1ImlE8ysNsVlPswPAuTQOsc130_head.
- NP331252.RAJPIc0nO1MtXNFyXgUJrJ1ImlE8ysNsVlPswPAuTQOsc130_assertion description "[Aicardi-Goutieres syndrome (AGS) (McKusick 225750) is an autosomal recessive disease with onset in the 1st year of life, resulting in progressive microcephaly, calcification of cerebral white matter, thalamus and basal ganglia, generalized cerebral demyelination and a chronic low-grade CSF lymphocytosis, without evidence of infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP331252.RAJPIc0nO1MtXNFyXgUJrJ1ImlE8ysNsVlPswPAuTQOsc130_provenance.
- NP331252.RAJPIc0nO1MtXNFyXgUJrJ1ImlE8ysNsVlPswPAuTQOsc130_assertion evidence source_evidence_literature NP331252.RAJPIc0nO1MtXNFyXgUJrJ1ImlE8ysNsVlPswPAuTQOsc130_provenance.
- NP331252.RAJPIc0nO1MtXNFyXgUJrJ1ImlE8ysNsVlPswPAuTQOsc130_assertion SIO_000772 10442562 NP331252.RAJPIc0nO1MtXNFyXgUJrJ1ImlE8ysNsVlPswPAuTQOsc130_provenance.
- NP331252.RAJPIc0nO1MtXNFyXgUJrJ1ImlE8ysNsVlPswPAuTQOsc130_assertion wasDerivedFrom befree-20150227 NP331252.RAJPIc0nO1MtXNFyXgUJrJ1ImlE8ysNsVlPswPAuTQOsc130_provenance.
- NP331252.RAJPIc0nO1MtXNFyXgUJrJ1ImlE8ysNsVlPswPAuTQOsc130_assertion wasGeneratedBy ECO_0000203 NP331252.RAJPIc0nO1MtXNFyXgUJrJ1ImlE8ysNsVlPswPAuTQOsc130_provenance.