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- source_evidence_literature type ECO_0000212 NP225773.RAbmvhFoJO5zMfqajl3EueEh057KSvpTyHqwL_Ldi-jkU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP225773.RAbmvhFoJO5zMfqajl3EueEh057KSvpTyHqwL_Ldi-jkU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP225773.RAbmvhFoJO5zMfqajl3EueEh057KSvpTyHqwL_Ldi-jkU130_provenance.
- NP225773.RAbmvhFoJO5zMfqajl3EueEh057KSvpTyHqwL_Ldi-jkU130_assertion description "[Recent work has demonstrated that more than 90% of patients with osteogenesis imperfecta (OI) have mutations in the gene for either the pro alpha 1 (I) chain or the gene for the pro alpha 2 (I) chain of type I procollagen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP225773.RAbmvhFoJO5zMfqajl3EueEh057KSvpTyHqwL_Ldi-jkU130_provenance.
- NP225773.RAbmvhFoJO5zMfqajl3EueEh057KSvpTyHqwL_Ldi-jkU130_assertion evidence source_evidence_literature NP225773.RAbmvhFoJO5zMfqajl3EueEh057KSvpTyHqwL_Ldi-jkU130_provenance.
- NP225773.RAbmvhFoJO5zMfqajl3EueEh057KSvpTyHqwL_Ldi-jkU130_assertion SIO_000772 7924138 NP225773.RAbmvhFoJO5zMfqajl3EueEh057KSvpTyHqwL_Ldi-jkU130_provenance.
- NP225773.RAbmvhFoJO5zMfqajl3EueEh057KSvpTyHqwL_Ldi-jkU130_assertion wasDerivedFrom befree-20150227 NP225773.RAbmvhFoJO5zMfqajl3EueEh057KSvpTyHqwL_Ldi-jkU130_provenance.
- NP225773.RAbmvhFoJO5zMfqajl3EueEh057KSvpTyHqwL_Ldi-jkU130_assertion wasGeneratedBy ECO_0000203 NP225773.RAbmvhFoJO5zMfqajl3EueEh057KSvpTyHqwL_Ldi-jkU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP225773.RAbmvhFoJO5zMfqajl3EueEh057KSvpTyHqwL_Ldi-jkU130_provenance.