Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP528319.RAqwc-bPimhLrMDzuFFTJNBg_FL00ah3E4i-mNoeP52jc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP528319.RAqwc-bPimhLrMDzuFFTJNBg_FL00ah3E4i-mNoeP52jc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP528319.RAqwc-bPimhLrMDzuFFTJNBg_FL00ah3E4i-mNoeP52jc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP528319.RAqwc-bPimhLrMDzuFFTJNBg_FL00ah3E4i-mNoeP52jc130_provenance.
- NP528319.RAqwc-bPimhLrMDzuFFTJNBg_FL00ah3E4i-mNoeP52jc130_assertion description "[To identify the genetic defect in Spanish families with Usher syndrome (USH) and probable involvement of the CLRN1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528319.RAqwc-bPimhLrMDzuFFTJNBg_FL00ah3E4i-mNoeP52jc130_provenance.
- NP528319.RAqwc-bPimhLrMDzuFFTJNBg_FL00ah3E4i-mNoeP52jc130_assertion evidence source_evidence_literature NP528319.RAqwc-bPimhLrMDzuFFTJNBg_FL00ah3E4i-mNoeP52jc130_provenance.
- NP528319.RAqwc-bPimhLrMDzuFFTJNBg_FL00ah3E4i-mNoeP52jc130_assertion SIO_000772 23304067 NP528319.RAqwc-bPimhLrMDzuFFTJNBg_FL00ah3E4i-mNoeP52jc130_provenance.
- NP528319.RAqwc-bPimhLrMDzuFFTJNBg_FL00ah3E4i-mNoeP52jc130_assertion wasDerivedFrom befree-20140225 NP528319.RAqwc-bPimhLrMDzuFFTJNBg_FL00ah3E4i-mNoeP52jc130_provenance.
- NP528319.RAqwc-bPimhLrMDzuFFTJNBg_FL00ah3E4i-mNoeP52jc130_assertion wasGeneratedBy ECO_0000203 NP528319.RAqwc-bPimhLrMDzuFFTJNBg_FL00ah3E4i-mNoeP52jc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP528319.RAqwc-bPimhLrMDzuFFTJNBg_FL00ah3E4i-mNoeP52jc130_provenance.