Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1267511.RAQIczKBcXsI1kd8yOzhPyv75J9Zyvik-QDKm08rqOyko130_assertion> ?p ?o ?g. }
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- NP1267511.RAQIczKBcXsI1kd8yOzhPyv75J9Zyvik-QDKm08rqOyko130_assertion type Assertion NP1267511.RAQIczKBcXsI1kd8yOzhPyv75J9Zyvik-QDKm08rqOyko130_head.
- NP1267511.RAQIczKBcXsI1kd8yOzhPyv75J9Zyvik-QDKm08rqOyko130_assertion description "[Here we briefly describe the human diseases so-far associated with mutations in TREX1, which include Aicardi-Gouti�res syndrome, familial chilblain lupus, systemic lupus erythematosus and retinal vasculopathy with cerebral leukodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1267511.RAQIczKBcXsI1kd8yOzhPyv75J9Zyvik-QDKm08rqOyko130_provenance.
- NP1267511.RAQIczKBcXsI1kd8yOzhPyv75J9Zyvik-QDKm08rqOyko130_assertion evidence source_evidence_literature NP1267511.RAQIczKBcXsI1kd8yOzhPyv75J9Zyvik-QDKm08rqOyko130_provenance.
- NP1267511.RAQIczKBcXsI1kd8yOzhPyv75J9Zyvik-QDKm08rqOyko130_assertion SIO_000772 25731743 NP1267511.RAQIczKBcXsI1kd8yOzhPyv75J9Zyvik-QDKm08rqOyko130_provenance.
- NP1267511.RAQIczKBcXsI1kd8yOzhPyv75J9Zyvik-QDKm08rqOyko130_assertion wasDerivedFrom befree-2016 NP1267511.RAQIczKBcXsI1kd8yOzhPyv75J9Zyvik-QDKm08rqOyko130_provenance.
- NP1267511.RAQIczKBcXsI1kd8yOzhPyv75J9Zyvik-QDKm08rqOyko130_assertion wasGeneratedBy ECO_0000203 NP1267511.RAQIczKBcXsI1kd8yOzhPyv75J9Zyvik-QDKm08rqOyko130_provenance.