Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1032001.RAfWyKi2sR91R6EGZXkD8yewL42njx3mdNHeUL4NMoRKw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1032001.RAfWyKi2sR91R6EGZXkD8yewL42njx3mdNHeUL4NMoRKw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1032001.RAfWyKi2sR91R6EGZXkD8yewL42njx3mdNHeUL4NMoRKw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1032001.RAfWyKi2sR91R6EGZXkD8yewL42njx3mdNHeUL4NMoRKw130_provenance.
- NP1032001.RAfWyKi2sR91R6EGZXkD8yewL42njx3mdNHeUL4NMoRKw130_assertion description "[Fabry disease is an X-linked lysosomal storage disorder due to deficient activity of alpha-galactosidase A (?-Gal A) leading to renal insufficiency in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1032001.RAfWyKi2sR91R6EGZXkD8yewL42njx3mdNHeUL4NMoRKw130_provenance.
- NP1032001.RAfWyKi2sR91R6EGZXkD8yewL42njx3mdNHeUL4NMoRKw130_assertion evidence source_evidence_literature NP1032001.RAfWyKi2sR91R6EGZXkD8yewL42njx3mdNHeUL4NMoRKw130_provenance.
- NP1032001.RAfWyKi2sR91R6EGZXkD8yewL42njx3mdNHeUL4NMoRKw130_assertion SIO_000772 23190516 NP1032001.RAfWyKi2sR91R6EGZXkD8yewL42njx3mdNHeUL4NMoRKw130_provenance.
- NP1032001.RAfWyKi2sR91R6EGZXkD8yewL42njx3mdNHeUL4NMoRKw130_assertion wasDerivedFrom befree-2016 NP1032001.RAfWyKi2sR91R6EGZXkD8yewL42njx3mdNHeUL4NMoRKw130_provenance.
- NP1032001.RAfWyKi2sR91R6EGZXkD8yewL42njx3mdNHeUL4NMoRKw130_assertion wasGeneratedBy ECO_0000203 NP1032001.RAfWyKi2sR91R6EGZXkD8yewL42njx3mdNHeUL4NMoRKw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1032001.RAfWyKi2sR91R6EGZXkD8yewL42njx3mdNHeUL4NMoRKw130_provenance.