Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP876064.RAvUwLdsk0nDi_RmQC80iNyiME8I9TMZgdhdvXwNG-bp8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP876064.RAvUwLdsk0nDi_RmQC80iNyiME8I9TMZgdhdvXwNG-bp8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP876064.RAvUwLdsk0nDi_RmQC80iNyiME8I9TMZgdhdvXwNG-bp8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP876064.RAvUwLdsk0nDi_RmQC80iNyiME8I9TMZgdhdvXwNG-bp8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP876064.RAvUwLdsk0nDi_RmQC80iNyiME8I9TMZgdhdvXwNG-bp8130_provenance.
- NP876064.RAvUwLdsk0nDi_RmQC80iNyiME8I9TMZgdhdvXwNG-bp8130_assertion wasGeneratedBy ECO_0000203 NP876064.RAvUwLdsk0nDi_RmQC80iNyiME8I9TMZgdhdvXwNG-bp8130_provenance.
- NP876064.RAvUwLdsk0nDi_RmQC80iNyiME8I9TMZgdhdvXwNG-bp8130_assertion wasDerivedFrom befree-20150227 NP876064.RAvUwLdsk0nDi_RmQC80iNyiME8I9TMZgdhdvXwNG-bp8130_provenance.
- NP876064.RAvUwLdsk0nDi_RmQC80iNyiME8I9TMZgdhdvXwNG-bp8130_assertion SIO_000772 20083694 NP876064.RAvUwLdsk0nDi_RmQC80iNyiME8I9TMZgdhdvXwNG-bp8130_provenance.
- NP876064.RAvUwLdsk0nDi_RmQC80iNyiME8I9TMZgdhdvXwNG-bp8130_assertion evidence source_evidence_literature NP876064.RAvUwLdsk0nDi_RmQC80iNyiME8I9TMZgdhdvXwNG-bp8130_provenance.
- NP876064.RAvUwLdsk0nDi_RmQC80iNyiME8I9TMZgdhdvXwNG-bp8130_assertion description "[Absence of LEMD3 mutation in the exons and splice sites of a family with BOS suggests that there is genetic heterogeneity for this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP876064.RAvUwLdsk0nDi_RmQC80iNyiME8I9TMZgdhdvXwNG-bp8130_provenance.