Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP769785.RAIAA9mcIHeM3ktM3-UuBWzMdUsJKwg5sfIxPmeso8XtQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP769785.RAIAA9mcIHeM3ktM3-UuBWzMdUsJKwg5sfIxPmeso8XtQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP769785.RAIAA9mcIHeM3ktM3-UuBWzMdUsJKwg5sfIxPmeso8XtQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP769785.RAIAA9mcIHeM3ktM3-UuBWzMdUsJKwg5sfIxPmeso8XtQ130_provenance.
- NP769785.RAIAA9mcIHeM3ktM3-UuBWzMdUsJKwg5sfIxPmeso8XtQ130_assertion description "[Homozygous mutations in ADAMTS10 and ADAMTS17 cause lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP769785.RAIAA9mcIHeM3ktM3-UuBWzMdUsJKwg5sfIxPmeso8XtQ130_provenance.
- NP769785.RAIAA9mcIHeM3ktM3-UuBWzMdUsJKwg5sfIxPmeso8XtQ130_assertion evidence source_evidence_literature NP769785.RAIAA9mcIHeM3ktM3-UuBWzMdUsJKwg5sfIxPmeso8XtQ130_provenance.
- NP769785.RAIAA9mcIHeM3ktM3-UuBWzMdUsJKwg5sfIxPmeso8XtQ130_assertion SIO_000772 19836009 NP769785.RAIAA9mcIHeM3ktM3-UuBWzMdUsJKwg5sfIxPmeso8XtQ130_provenance.
- NP769785.RAIAA9mcIHeM3ktM3-UuBWzMdUsJKwg5sfIxPmeso8XtQ130_assertion wasDerivedFrom befree-2016 NP769785.RAIAA9mcIHeM3ktM3-UuBWzMdUsJKwg5sfIxPmeso8XtQ130_provenance.
- NP769785.RAIAA9mcIHeM3ktM3-UuBWzMdUsJKwg5sfIxPmeso8XtQ130_assertion wasGeneratedBy ECO_0000203 NP769785.RAIAA9mcIHeM3ktM3-UuBWzMdUsJKwg5sfIxPmeso8XtQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP769785.RAIAA9mcIHeM3ktM3-UuBWzMdUsJKwg5sfIxPmeso8XtQ130_provenance.