Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP290800.RATQ15_l9PQbLXSc3ADYajgd9R1mOApAkUyoJ6b84DjD8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP290800.RATQ15_l9PQbLXSc3ADYajgd9R1mOApAkUyoJ6b84DjD8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP290800.RATQ15_l9PQbLXSc3ADYajgd9R1mOApAkUyoJ6b84DjD8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP290800.RATQ15_l9PQbLXSc3ADYajgd9R1mOApAkUyoJ6b84DjD8130_provenance.
- NP290800.RATQ15_l9PQbLXSc3ADYajgd9R1mOApAkUyoJ6b84DjD8130_assertion description "[Kjellin syndrome is characterized by central retinal degeneration in addition to ARHSP-TCC and the disease is associated with mutations in the SPG15 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP290800.RATQ15_l9PQbLXSc3ADYajgd9R1mOApAkUyoJ6b84DjD8130_provenance.
- NP290800.RATQ15_l9PQbLXSc3ADYajgd9R1mOApAkUyoJ6b84DjD8130_assertion evidence source_evidence_literature NP290800.RATQ15_l9PQbLXSc3ADYajgd9R1mOApAkUyoJ6b84DjD8130_provenance.
- NP290800.RATQ15_l9PQbLXSc3ADYajgd9R1mOApAkUyoJ6b84DjD8130_assertion SIO_000772 19194956 NP290800.RATQ15_l9PQbLXSc3ADYajgd9R1mOApAkUyoJ6b84DjD8130_provenance.
- NP290800.RATQ15_l9PQbLXSc3ADYajgd9R1mOApAkUyoJ6b84DjD8130_assertion wasDerivedFrom befree-20140225 NP290800.RATQ15_l9PQbLXSc3ADYajgd9R1mOApAkUyoJ6b84DjD8130_provenance.
- NP290800.RATQ15_l9PQbLXSc3ADYajgd9R1mOApAkUyoJ6b84DjD8130_assertion wasGeneratedBy ECO_0000203 NP290800.RATQ15_l9PQbLXSc3ADYajgd9R1mOApAkUyoJ6b84DjD8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP290800.RATQ15_l9PQbLXSc3ADYajgd9R1mOApAkUyoJ6b84DjD8130_provenance.