Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP343009.RAsSU7bgEyPMrXWpfwImSs3sqaoSVyq_hY8KoQaSdzLMo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP343009.RAsSU7bgEyPMrXWpfwImSs3sqaoSVyq_hY8KoQaSdzLMo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP343009.RAsSU7bgEyPMrXWpfwImSs3sqaoSVyq_hY8KoQaSdzLMo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP343009.RAsSU7bgEyPMrXWpfwImSs3sqaoSVyq_hY8KoQaSdzLMo130_provenance.
- NP343009.RAsSU7bgEyPMrXWpfwImSs3sqaoSVyq_hY8KoQaSdzLMo130_assertion description "[Deletion of Xpter encompassing the SHOX gene and PAR1 region in familial patients with Leri-Weill Dyschondrosteosis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343009.RAsSU7bgEyPMrXWpfwImSs3sqaoSVyq_hY8KoQaSdzLMo130_provenance.
- NP343009.RAsSU7bgEyPMrXWpfwImSs3sqaoSVyq_hY8KoQaSdzLMo130_assertion evidence source_evidence_literature NP343009.RAsSU7bgEyPMrXWpfwImSs3sqaoSVyq_hY8KoQaSdzLMo130_provenance.
- NP343009.RAsSU7bgEyPMrXWpfwImSs3sqaoSVyq_hY8KoQaSdzLMo130_assertion SIO_000772 19400538 NP343009.RAsSU7bgEyPMrXWpfwImSs3sqaoSVyq_hY8KoQaSdzLMo130_provenance.
- NP343009.RAsSU7bgEyPMrXWpfwImSs3sqaoSVyq_hY8KoQaSdzLMo130_assertion wasDerivedFrom befree-20140225 NP343009.RAsSU7bgEyPMrXWpfwImSs3sqaoSVyq_hY8KoQaSdzLMo130_provenance.
- NP343009.RAsSU7bgEyPMrXWpfwImSs3sqaoSVyq_hY8KoQaSdzLMo130_assertion wasGeneratedBy ECO_0000203 NP343009.RAsSU7bgEyPMrXWpfwImSs3sqaoSVyq_hY8KoQaSdzLMo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP343009.RAsSU7bgEyPMrXWpfwImSs3sqaoSVyq_hY8KoQaSdzLMo130_provenance.