Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP990933.RA1x2nz4tM1tg_vjXkpozbmB-3q9svVoJgoyeFH7LVUYA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP990933.RA1x2nz4tM1tg_vjXkpozbmB-3q9svVoJgoyeFH7LVUYA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP990933.RA1x2nz4tM1tg_vjXkpozbmB-3q9svVoJgoyeFH7LVUYA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP990933.RA1x2nz4tM1tg_vjXkpozbmB-3q9svVoJgoyeFH7LVUYA130_provenance.
- NP990933.RA1x2nz4tM1tg_vjXkpozbmB-3q9svVoJgoyeFH7LVUYA130_assertion description "[This figure is comparable to the percentage of RP2 gene mutations that we have detected in our entire XLRP patient pool (10%-15%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990933.RA1x2nz4tM1tg_vjXkpozbmB-3q9svVoJgoyeFH7LVUYA130_provenance.
- NP990933.RA1x2nz4tM1tg_vjXkpozbmB-3q9svVoJgoyeFH7LVUYA130_assertion evidence source_evidence_literature NP990933.RA1x2nz4tM1tg_vjXkpozbmB-3q9svVoJgoyeFH7LVUYA130_provenance.
- NP990933.RA1x2nz4tM1tg_vjXkpozbmB-3q9svVoJgoyeFH7LVUYA130_assertion SIO_000772 10480356 NP990933.RA1x2nz4tM1tg_vjXkpozbmB-3q9svVoJgoyeFH7LVUYA130_provenance.
- NP990933.RA1x2nz4tM1tg_vjXkpozbmB-3q9svVoJgoyeFH7LVUYA130_assertion wasDerivedFrom befree-20150227 NP990933.RA1x2nz4tM1tg_vjXkpozbmB-3q9svVoJgoyeFH7LVUYA130_provenance.
- NP990933.RA1x2nz4tM1tg_vjXkpozbmB-3q9svVoJgoyeFH7LVUYA130_assertion wasGeneratedBy ECO_0000203 NP990933.RA1x2nz4tM1tg_vjXkpozbmB-3q9svVoJgoyeFH7LVUYA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP990933.RA1x2nz4tM1tg_vjXkpozbmB-3q9svVoJgoyeFH7LVUYA130_provenance.