Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1027735.RAQ4-Q96pcfNPnB35K57fzD60ocBbeUxp2Ix4A4C-gu3I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1027735.RAQ4-Q96pcfNPnB35K57fzD60ocBbeUxp2Ix4A4C-gu3I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1027735.RAQ4-Q96pcfNPnB35K57fzD60ocBbeUxp2Ix4A4C-gu3I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1027735.RAQ4-Q96pcfNPnB35K57fzD60ocBbeUxp2Ix4A4C-gu3I130_provenance.
- befree-2016 importedOn "2016-02-19" NP1027735.RAQ4-Q96pcfNPnB35K57fzD60ocBbeUxp2Ix4A4C-gu3I130_provenance.
- NP1027735.RAQ4-Q96pcfNPnB35K57fzD60ocBbeUxp2Ix4A4C-gu3I130_assertion wasGeneratedBy ECO_0000203 NP1027735.RAQ4-Q96pcfNPnB35K57fzD60ocBbeUxp2Ix4A4C-gu3I130_provenance.
- NP1027735.RAQ4-Q96pcfNPnB35K57fzD60ocBbeUxp2Ix4A4C-gu3I130_assertion wasDerivedFrom befree-2016 NP1027735.RAQ4-Q96pcfNPnB35K57fzD60ocBbeUxp2Ix4A4C-gu3I130_provenance.
- NP1027735.RAQ4-Q96pcfNPnB35K57fzD60ocBbeUxp2Ix4A4C-gu3I130_assertion SIO_000772 23144630 NP1027735.RAQ4-Q96pcfNPnB35K57fzD60ocBbeUxp2Ix4A4C-gu3I130_provenance.
- NP1027735.RAQ4-Q96pcfNPnB35K57fzD60ocBbeUxp2Ix4A4C-gu3I130_assertion evidence source_evidence_literature NP1027735.RAQ4-Q96pcfNPnB35K57fzD60ocBbeUxp2Ix4A4C-gu3I130_provenance.
- NP1027735.RAQ4-Q96pcfNPnB35K57fzD60ocBbeUxp2Ix4A4C-gu3I130_assertion description "[Heterozygous mutations in the PRPF31 gene cause autosomal dominant retinitis pigmentosa (adRP), a hereditary disorder leading to progressive blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1027735.RAQ4-Q96pcfNPnB35K57fzD60ocBbeUxp2Ix4A4C-gu3I130_provenance.