Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP393615.RAg1h3SHRojKAFsUpZPwtlk3mo-nGJCdScCfVz5tskFZ8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP393615.RAg1h3SHRojKAFsUpZPwtlk3mo-nGJCdScCfVz5tskFZ8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP393615.RAg1h3SHRojKAFsUpZPwtlk3mo-nGJCdScCfVz5tskFZ8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP393615.RAg1h3SHRojKAFsUpZPwtlk3mo-nGJCdScCfVz5tskFZ8130_provenance.
- befree-2016 importedOn "2016-02-19" NP393615.RAg1h3SHRojKAFsUpZPwtlk3mo-nGJCdScCfVz5tskFZ8130_provenance.
- NP393615.RAg1h3SHRojKAFsUpZPwtlk3mo-nGJCdScCfVz5tskFZ8130_assertion wasGeneratedBy ECO_0000203 NP393615.RAg1h3SHRojKAFsUpZPwtlk3mo-nGJCdScCfVz5tskFZ8130_provenance.
- NP393615.RAg1h3SHRojKAFsUpZPwtlk3mo-nGJCdScCfVz5tskFZ8130_assertion wasDerivedFrom befree-2016 NP393615.RAg1h3SHRojKAFsUpZPwtlk3mo-nGJCdScCfVz5tskFZ8130_provenance.
- NP393615.RAg1h3SHRojKAFsUpZPwtlk3mo-nGJCdScCfVz5tskFZ8130_assertion SIO_000772 12736871 NP393615.RAg1h3SHRojKAFsUpZPwtlk3mo-nGJCdScCfVz5tskFZ8130_provenance.
- NP393615.RAg1h3SHRojKAFsUpZPwtlk3mo-nGJCdScCfVz5tskFZ8130_assertion evidence source_evidence_literature NP393615.RAg1h3SHRojKAFsUpZPwtlk3mo-nGJCdScCfVz5tskFZ8130_provenance.
- NP393615.RAg1h3SHRojKAFsUpZPwtlk3mo-nGJCdScCfVz5tskFZ8130_assertion description "[Genomewide significance was reached for a locus on chromosome 2 for patients with affected CMC1 joints (LOD = 4.97); this locus was also significant for patients with OA in both CMC1 and DIP joints (LOD = 4.44).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP393615.RAg1h3SHRojKAFsUpZPwtlk3mo-nGJCdScCfVz5tskFZ8130_provenance.