Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP225939.RApYWSgZaK4MJIshVdzWtlJMQwDnkFrLkGMjElLOvZ6TM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP225939.RApYWSgZaK4MJIshVdzWtlJMQwDnkFrLkGMjElLOvZ6TM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP225939.RApYWSgZaK4MJIshVdzWtlJMQwDnkFrLkGMjElLOvZ6TM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP225939.RApYWSgZaK4MJIshVdzWtlJMQwDnkFrLkGMjElLOvZ6TM130_provenance.
- NP225939.RApYWSgZaK4MJIshVdzWtlJMQwDnkFrLkGMjElLOvZ6TM130_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." NP225939.RApYWSgZaK4MJIshVdzWtlJMQwDnkFrLkGMjElLOvZ6TM130_provenance.
- NP225939.RApYWSgZaK4MJIshVdzWtlJMQwDnkFrLkGMjElLOvZ6TM130_assertion evidence source_evidence_literature NP225939.RApYWSgZaK4MJIshVdzWtlJMQwDnkFrLkGMjElLOvZ6TM130_provenance.
- NP225939.RApYWSgZaK4MJIshVdzWtlJMQwDnkFrLkGMjElLOvZ6TM130_assertion SIO_000772 2572730 NP225939.RApYWSgZaK4MJIshVdzWtlJMQwDnkFrLkGMjElLOvZ6TM130_provenance.
- NP225939.RApYWSgZaK4MJIshVdzWtlJMQwDnkFrLkGMjElLOvZ6TM130_assertion wasDerivedFrom befree-20150227 NP225939.RApYWSgZaK4MJIshVdzWtlJMQwDnkFrLkGMjElLOvZ6TM130_provenance.
- NP225939.RApYWSgZaK4MJIshVdzWtlJMQwDnkFrLkGMjElLOvZ6TM130_assertion wasGeneratedBy ECO_0000203 NP225939.RApYWSgZaK4MJIshVdzWtlJMQwDnkFrLkGMjElLOvZ6TM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP225939.RApYWSgZaK4MJIshVdzWtlJMQwDnkFrLkGMjElLOvZ6TM130_provenance.