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- source_evidence_literature type ECO_0000212 NP920873.RAicnOq9rAArtMyLkDzxSpp77cv_ErGThA-ETaoilzkJc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP920873.RAicnOq9rAArtMyLkDzxSpp77cv_ErGThA-ETaoilzkJc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP920873.RAicnOq9rAArtMyLkDzxSpp77cv_ErGThA-ETaoilzkJc130_provenance.
- NP920873.RAicnOq9rAArtMyLkDzxSpp77cv_ErGThA-ETaoilzkJc130_assertion description "[Camurati-Engelmann disease (CED, MIM 131300) is an autosomal dominant, progressive diaphyseal dysplasia characterized by hyperosteosis and sclerosis of the diaphyses of long bones.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP920873.RAicnOq9rAArtMyLkDzxSpp77cv_ErGThA-ETaoilzkJc130_provenance.
- NP920873.RAicnOq9rAArtMyLkDzxSpp77cv_ErGThA-ETaoilzkJc130_assertion evidence source_evidence_literature NP920873.RAicnOq9rAArtMyLkDzxSpp77cv_ErGThA-ETaoilzkJc130_provenance.
- NP920873.RAicnOq9rAArtMyLkDzxSpp77cv_ErGThA-ETaoilzkJc130_assertion SIO_000772 10973241 NP920873.RAicnOq9rAArtMyLkDzxSpp77cv_ErGThA-ETaoilzkJc130_provenance.
- NP920873.RAicnOq9rAArtMyLkDzxSpp77cv_ErGThA-ETaoilzkJc130_assertion wasDerivedFrom befree-20150227 NP920873.RAicnOq9rAArtMyLkDzxSpp77cv_ErGThA-ETaoilzkJc130_provenance.
- NP920873.RAicnOq9rAArtMyLkDzxSpp77cv_ErGThA-ETaoilzkJc130_assertion wasGeneratedBy ECO_0000203 NP920873.RAicnOq9rAArtMyLkDzxSpp77cv_ErGThA-ETaoilzkJc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP920873.RAicnOq9rAArtMyLkDzxSpp77cv_ErGThA-ETaoilzkJc130_provenance.