Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP816981.RAGSoql3-TM1731vvXHS7FyzgaRkCDYIEREbchb9exyqM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP816981.RAGSoql3-TM1731vvXHS7FyzgaRkCDYIEREbchb9exyqM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP816981.RAGSoql3-TM1731vvXHS7FyzgaRkCDYIEREbchb9exyqM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP816981.RAGSoql3-TM1731vvXHS7FyzgaRkCDYIEREbchb9exyqM130_provenance.
- NP816981.RAGSoql3-TM1731vvXHS7FyzgaRkCDYIEREbchb9exyqM130_assertion description "[Mutations in RP2 cause the second most frequent form of X-linked retinitis pigmentosa, a severe retinal degeneration that leads to loss of visual acuity and blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP816981.RAGSoql3-TM1731vvXHS7FyzgaRkCDYIEREbchb9exyqM130_provenance.
- NP816981.RAGSoql3-TM1731vvXHS7FyzgaRkCDYIEREbchb9exyqM130_assertion evidence source_evidence_literature NP816981.RAGSoql3-TM1731vvXHS7FyzgaRkCDYIEREbchb9exyqM130_provenance.
- NP816981.RAGSoql3-TM1731vvXHS7FyzgaRkCDYIEREbchb9exyqM130_assertion SIO_000772 11371510 NP816981.RAGSoql3-TM1731vvXHS7FyzgaRkCDYIEREbchb9exyqM130_provenance.
- NP816981.RAGSoql3-TM1731vvXHS7FyzgaRkCDYIEREbchb9exyqM130_assertion wasDerivedFrom befree-20140225 NP816981.RAGSoql3-TM1731vvXHS7FyzgaRkCDYIEREbchb9exyqM130_provenance.
- NP816981.RAGSoql3-TM1731vvXHS7FyzgaRkCDYIEREbchb9exyqM130_assertion wasGeneratedBy ECO_0000203 NP816981.RAGSoql3-TM1731vvXHS7FyzgaRkCDYIEREbchb9exyqM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP816981.RAGSoql3-TM1731vvXHS7FyzgaRkCDYIEREbchb9exyqM130_provenance.