Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP591205.RAaj9nHrvmGXy6QGILUYSVETqdaWDUaAXkhFpcZ5xWKyU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP591205.RAaj9nHrvmGXy6QGILUYSVETqdaWDUaAXkhFpcZ5xWKyU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP591205.RAaj9nHrvmGXy6QGILUYSVETqdaWDUaAXkhFpcZ5xWKyU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP591205.RAaj9nHrvmGXy6QGILUYSVETqdaWDUaAXkhFpcZ5xWKyU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP591205.RAaj9nHrvmGXy6QGILUYSVETqdaWDUaAXkhFpcZ5xWKyU130_provenance.
- NP591205.RAaj9nHrvmGXy6QGILUYSVETqdaWDUaAXkhFpcZ5xWKyU130_assertion wasGeneratedBy ECO_0000203 NP591205.RAaj9nHrvmGXy6QGILUYSVETqdaWDUaAXkhFpcZ5xWKyU130_provenance.
- NP591205.RAaj9nHrvmGXy6QGILUYSVETqdaWDUaAXkhFpcZ5xWKyU130_assertion wasDerivedFrom befree-20150227 NP591205.RAaj9nHrvmGXy6QGILUYSVETqdaWDUaAXkhFpcZ5xWKyU130_provenance.
- NP591205.RAaj9nHrvmGXy6QGILUYSVETqdaWDUaAXkhFpcZ5xWKyU130_assertion SIO_000772 21734245 NP591205.RAaj9nHrvmGXy6QGILUYSVETqdaWDUaAXkhFpcZ5xWKyU130_provenance.
- NP591205.RAaj9nHrvmGXy6QGILUYSVETqdaWDUaAXkhFpcZ5xWKyU130_assertion evidence source_evidence_literature NP591205.RAaj9nHrvmGXy6QGILUYSVETqdaWDUaAXkhFpcZ5xWKyU130_provenance.
- NP591205.RAaj9nHrvmGXy6QGILUYSVETqdaWDUaAXkhFpcZ5xWKyU130_assertion description "[Hypomorphic mutations in the X-linked NEMO gene and hypermorphic mutations in the autosomal IKBA gene cause X-linked recessive and autosomal dominant anhidrotic ectodermal dysplasia with immunodeficiency (EDA-ID) syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP591205.RAaj9nHrvmGXy6QGILUYSVETqdaWDUaAXkhFpcZ5xWKyU130_provenance.