Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_provenance.
- NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_assertion description "[There is now strong evidence for the implication of collagen alpha 1(I), alpha 2(I) and alpha 1(III) mutations in many forms of osteogenesis imperfecta and inherited arterial aneurysms (Ehlers Danlos syndrome type IV).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_provenance.
- NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_assertion evidence source_evidence_literature NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_provenance.
- NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_assertion SIO_000772 2572730 NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_provenance.
- NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_assertion wasDerivedFrom befree-20140225 NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_provenance.
- NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_assertion wasGeneratedBy ECO_0000203 NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP719280.RACm6sIR0o_pDyFaTWm1yDIvjjpkQz7SCY9znnQ60X6WE130_provenance.