Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP638402.RAWdQinoP25AhHd8gWrLB-0rmCZ8xHCoQi0Jdqm6ZBVQk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP638402.RAWdQinoP25AhHd8gWrLB-0rmCZ8xHCoQi0Jdqm6ZBVQk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP638402.RAWdQinoP25AhHd8gWrLB-0rmCZ8xHCoQi0Jdqm6ZBVQk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP638402.RAWdQinoP25AhHd8gWrLB-0rmCZ8xHCoQi0Jdqm6ZBVQk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP638402.RAWdQinoP25AhHd8gWrLB-0rmCZ8xHCoQi0Jdqm6ZBVQk130_provenance.
- NP638402.RAWdQinoP25AhHd8gWrLB-0rmCZ8xHCoQi0Jdqm6ZBVQk130_assertion wasGeneratedBy ECO_0000203 NP638402.RAWdQinoP25AhHd8gWrLB-0rmCZ8xHCoQi0Jdqm6ZBVQk130_provenance.
- NP638402.RAWdQinoP25AhHd8gWrLB-0rmCZ8xHCoQi0Jdqm6ZBVQk130_assertion wasDerivedFrom befree-20150227 NP638402.RAWdQinoP25AhHd8gWrLB-0rmCZ8xHCoQi0Jdqm6ZBVQk130_provenance.
- NP638402.RAWdQinoP25AhHd8gWrLB-0rmCZ8xHCoQi0Jdqm6ZBVQk130_assertion SIO_000772 21667357 NP638402.RAWdQinoP25AhHd8gWrLB-0rmCZ8xHCoQi0Jdqm6ZBVQk130_provenance.
- NP638402.RAWdQinoP25AhHd8gWrLB-0rmCZ8xHCoQi0Jdqm6ZBVQk130_assertion evidence source_evidence_literature NP638402.RAWdQinoP25AhHd8gWrLB-0rmCZ8xHCoQi0Jdqm6ZBVQk130_provenance.
- NP638402.RAWdQinoP25AhHd8gWrLB-0rmCZ8xHCoQi0Jdqm6ZBVQk130_assertion description "[Dominant inheritance of osteogenesis imperfecta (OI) is caused by mutations in COL1A1 or COL1A2, the genes that encode type I collagen, and CRTAP, LEPRE1, PPIB, FKBP10, SERPINH1, and SP7 mutations were recently detected in a minority of patients with autosomal recessive OI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP638402.RAWdQinoP25AhHd8gWrLB-0rmCZ8xHCoQi0Jdqm6ZBVQk130_provenance.