Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP880348.RAEZo80-jbGvABPVrbS4NHjRwG7waE0eWOtvZLm0MuoFw130_assertion> ?p ?o ?g. }
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- NP880348.RAEZo80-jbGvABPVrbS4NHjRwG7waE0eWOtvZLm0MuoFw130_assertion type Assertion NP880348.RAEZo80-jbGvABPVrbS4NHjRwG7waE0eWOtvZLm0MuoFw130_head.
- NP880348.RAEZo80-jbGvABPVrbS4NHjRwG7waE0eWOtvZLm0MuoFw130_assertion wasGeneratedBy ECO_0000203 NP880348.RAEZo80-jbGvABPVrbS4NHjRwG7waE0eWOtvZLm0MuoFw130_provenance.
- NP880348.RAEZo80-jbGvABPVrbS4NHjRwG7waE0eWOtvZLm0MuoFw130_assertion wasDerivedFrom befree-20150227 NP880348.RAEZo80-jbGvABPVrbS4NHjRwG7waE0eWOtvZLm0MuoFw130_provenance.
- NP880348.RAEZo80-jbGvABPVrbS4NHjRwG7waE0eWOtvZLm0MuoFw130_assertion SIO_000772 24335234 NP880348.RAEZo80-jbGvABPVrbS4NHjRwG7waE0eWOtvZLm0MuoFw130_provenance.
- NP880348.RAEZo80-jbGvABPVrbS4NHjRwG7waE0eWOtvZLm0MuoFw130_assertion evidence source_evidence_literature NP880348.RAEZo80-jbGvABPVrbS4NHjRwG7waE0eWOtvZLm0MuoFw130_provenance.
- NP880348.RAEZo80-jbGvABPVrbS4NHjRwG7waE0eWOtvZLm0MuoFw130_assertion description "[Germ-line mutations in SAMHD1 have been described in patients with Aicardi-Goutières syndrome (AGS), a congenital autoimmune disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP880348.RAEZo80-jbGvABPVrbS4NHjRwG7waE0eWOtvZLm0MuoFw130_provenance.