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- source_evidence_literature type ECO_0000212 NP234866.RAp9L6ASuZ9AU1yNhhb7CxmTjkgVZO2pIDSJfxKAnROAk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP234866.RAp9L6ASuZ9AU1yNhhb7CxmTjkgVZO2pIDSJfxKAnROAk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP234866.RAp9L6ASuZ9AU1yNhhb7CxmTjkgVZO2pIDSJfxKAnROAk130_provenance.
- NP234866.RAp9L6ASuZ9AU1yNhhb7CxmTjkgVZO2pIDSJfxKAnROAk130_assertion description "[Using a combination of homozygosity mapping, exome sequencing, and Sanger sequencing, we identified homozygosity for one splice-site and two missense mutations in the gene encoding the A3 isoform of the aldehyde dehydrogenase 1 (ALDH1A3) in three consanguineous families segregating A/M with occasional orbital cystic, neurological, and cardiac anomalies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP234866.RAp9L6ASuZ9AU1yNhhb7CxmTjkgVZO2pIDSJfxKAnROAk130_provenance.
- NP234866.RAp9L6ASuZ9AU1yNhhb7CxmTjkgVZO2pIDSJfxKAnROAk130_assertion evidence source_evidence_literature NP234866.RAp9L6ASuZ9AU1yNhhb7CxmTjkgVZO2pIDSJfxKAnROAk130_provenance.
- NP234866.RAp9L6ASuZ9AU1yNhhb7CxmTjkgVZO2pIDSJfxKAnROAk130_assertion SIO_000772 23312594 NP234866.RAp9L6ASuZ9AU1yNhhb7CxmTjkgVZO2pIDSJfxKAnROAk130_provenance.
- NP234866.RAp9L6ASuZ9AU1yNhhb7CxmTjkgVZO2pIDSJfxKAnROAk130_assertion wasDerivedFrom befree-20150227 NP234866.RAp9L6ASuZ9AU1yNhhb7CxmTjkgVZO2pIDSJfxKAnROAk130_provenance.
- NP234866.RAp9L6ASuZ9AU1yNhhb7CxmTjkgVZO2pIDSJfxKAnROAk130_assertion wasGeneratedBy ECO_0000203 NP234866.RAp9L6ASuZ9AU1yNhhb7CxmTjkgVZO2pIDSJfxKAnROAk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP234866.RAp9L6ASuZ9AU1yNhhb7CxmTjkgVZO2pIDSJfxKAnROAk130_provenance.