Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP582288.RAtWZ0458-BAoLEGZVosB9kq6b3TzfI7sP1ckXC0m3bgE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP582288.RAtWZ0458-BAoLEGZVosB9kq6b3TzfI7sP1ckXC0m3bgE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP582288.RAtWZ0458-BAoLEGZVosB9kq6b3TzfI7sP1ckXC0m3bgE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP582288.RAtWZ0458-BAoLEGZVosB9kq6b3TzfI7sP1ckXC0m3bgE130_provenance.
- NP582288.RAtWZ0458-BAoLEGZVosB9kq6b3TzfI7sP1ckXC0m3bgE130_assertion description "[The majority of remaining affected individuals have recessively inherited forms of OI with the causative variants in the more recently discovered genes CRTAP, FKBP10, LEPRE1,PLOD2, PPIB, SERPINF1, SERPINH1 and SP7, or in other yet undiscovered genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP582288.RAtWZ0458-BAoLEGZVosB9kq6b3TzfI7sP1ckXC0m3bgE130_provenance.
- NP582288.RAtWZ0458-BAoLEGZVosB9kq6b3TzfI7sP1ckXC0m3bgE130_assertion evidence source_evidence_literature NP582288.RAtWZ0458-BAoLEGZVosB9kq6b3TzfI7sP1ckXC0m3bgE130_provenance.
- NP582288.RAtWZ0458-BAoLEGZVosB9kq6b3TzfI7sP1ckXC0m3bgE130_assertion SIO_000772 21829228 NP582288.RAtWZ0458-BAoLEGZVosB9kq6b3TzfI7sP1ckXC0m3bgE130_provenance.
- NP582288.RAtWZ0458-BAoLEGZVosB9kq6b3TzfI7sP1ckXC0m3bgE130_assertion wasDerivedFrom befree-20140225 NP582288.RAtWZ0458-BAoLEGZVosB9kq6b3TzfI7sP1ckXC0m3bgE130_provenance.
- NP582288.RAtWZ0458-BAoLEGZVosB9kq6b3TzfI7sP1ckXC0m3bgE130_assertion wasGeneratedBy ECO_0000203 NP582288.RAtWZ0458-BAoLEGZVosB9kq6b3TzfI7sP1ckXC0m3bgE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP582288.RAtWZ0458-BAoLEGZVosB9kq6b3TzfI7sP1ckXC0m3bgE130_provenance.