Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP223035.RAhxDcakNpFrtNboaeJZRIyIIfmQi4ZQCWJn4B_5W9tYg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP223035.RAhxDcakNpFrtNboaeJZRIyIIfmQi4ZQCWJn4B_5W9tYg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP223035.RAhxDcakNpFrtNboaeJZRIyIIfmQi4ZQCWJn4B_5W9tYg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP223035.RAhxDcakNpFrtNboaeJZRIyIIfmQi4ZQCWJn4B_5W9tYg130_provenance.
- NP223035.RAhxDcakNpFrtNboaeJZRIyIIfmQi4ZQCWJn4B_5W9tYg130_assertion description "[We recently observed mutations in ADAR1 to cause a phenotype of bilateral striatal necrosis (BSN) in a child with the type I interferonopathy Aicardi-Gouti�res syndrome (AGS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP223035.RAhxDcakNpFrtNboaeJZRIyIIfmQi4ZQCWJn4B_5W9tYg130_provenance.
- NP223035.RAhxDcakNpFrtNboaeJZRIyIIfmQi4ZQCWJn4B_5W9tYg130_assertion evidence source_evidence_literature NP223035.RAhxDcakNpFrtNboaeJZRIyIIfmQi4ZQCWJn4B_5W9tYg130_provenance.
- NP223035.RAhxDcakNpFrtNboaeJZRIyIIfmQi4ZQCWJn4B_5W9tYg130_assertion SIO_000772 24262145 NP223035.RAhxDcakNpFrtNboaeJZRIyIIfmQi4ZQCWJn4B_5W9tYg130_provenance.
- NP223035.RAhxDcakNpFrtNboaeJZRIyIIfmQi4ZQCWJn4B_5W9tYg130_assertion wasDerivedFrom befree-20150227 NP223035.RAhxDcakNpFrtNboaeJZRIyIIfmQi4ZQCWJn4B_5W9tYg130_provenance.
- NP223035.RAhxDcakNpFrtNboaeJZRIyIIfmQi4ZQCWJn4B_5W9tYg130_assertion wasGeneratedBy ECO_0000203 NP223035.RAhxDcakNpFrtNboaeJZRIyIIfmQi4ZQCWJn4B_5W9tYg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP223035.RAhxDcakNpFrtNboaeJZRIyIIfmQi4ZQCWJn4B_5W9tYg130_provenance.