Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP968908.RAj69Y7VgeqSKJGAWht9yWMRqkiDjfiN6h94vc2rLgfAM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP968908.RAj69Y7VgeqSKJGAWht9yWMRqkiDjfiN6h94vc2rLgfAM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP968908.RAj69Y7VgeqSKJGAWht9yWMRqkiDjfiN6h94vc2rLgfAM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP968908.RAj69Y7VgeqSKJGAWht9yWMRqkiDjfiN6h94vc2rLgfAM130_provenance.
- NP968908.RAj69Y7VgeqSKJGAWht9yWMRqkiDjfiN6h94vc2rLgfAM130_assertion description "[Hypohidrotic ectodermal dysplasia (HED) can be caused by mutations in the X-linked ectodysplasin A (ED1) gene or the autosomal ectodysplasin A-receptor (EDAR) and EDAR-associated death domain (EDARADD) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP968908.RAj69Y7VgeqSKJGAWht9yWMRqkiDjfiN6h94vc2rLgfAM130_provenance.
- NP968908.RAj69Y7VgeqSKJGAWht9yWMRqkiDjfiN6h94vc2rLgfAM130_assertion evidence source_evidence_literature NP968908.RAj69Y7VgeqSKJGAWht9yWMRqkiDjfiN6h94vc2rLgfAM130_provenance.
- NP968908.RAj69Y7VgeqSKJGAWht9yWMRqkiDjfiN6h94vc2rLgfAM130_assertion SIO_000772 18231121 NP968908.RAj69Y7VgeqSKJGAWht9yWMRqkiDjfiN6h94vc2rLgfAM130_provenance.
- NP968908.RAj69Y7VgeqSKJGAWht9yWMRqkiDjfiN6h94vc2rLgfAM130_assertion wasDerivedFrom befree-20150227 NP968908.RAj69Y7VgeqSKJGAWht9yWMRqkiDjfiN6h94vc2rLgfAM130_provenance.
- NP968908.RAj69Y7VgeqSKJGAWht9yWMRqkiDjfiN6h94vc2rLgfAM130_assertion wasGeneratedBy ECO_0000203 NP968908.RAj69Y7VgeqSKJGAWht9yWMRqkiDjfiN6h94vc2rLgfAM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP968908.RAj69Y7VgeqSKJGAWht9yWMRqkiDjfiN6h94vc2rLgfAM130_provenance.