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- source_evidence_literature type ECO_0000212 NP810494.RAv-iTy63E3kFjAWdhWvnle1-hSEB7LUsMwpyLJD8QVfk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP810494.RAv-iTy63E3kFjAWdhWvnle1-hSEB7LUsMwpyLJD8QVfk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP810494.RAv-iTy63E3kFjAWdhWvnle1-hSEB7LUsMwpyLJD8QVfk130_provenance.
- NP810494.RAv-iTy63E3kFjAWdhWvnle1-hSEB7LUsMwpyLJD8QVfk130_assertion description "[Identification of novel EIF2B mutations in Chinese patients with vanishing white matter disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP810494.RAv-iTy63E3kFjAWdhWvnle1-hSEB7LUsMwpyLJD8QVfk130_provenance.
- NP810494.RAv-iTy63E3kFjAWdhWvnle1-hSEB7LUsMwpyLJD8QVfk130_assertion evidence source_evidence_literature NP810494.RAv-iTy63E3kFjAWdhWvnle1-hSEB7LUsMwpyLJD8QVfk130_provenance.
- NP810494.RAv-iTy63E3kFjAWdhWvnle1-hSEB7LUsMwpyLJD8QVfk130_assertion SIO_000772 19158808 NP810494.RAv-iTy63E3kFjAWdhWvnle1-hSEB7LUsMwpyLJD8QVfk130_provenance.
- NP810494.RAv-iTy63E3kFjAWdhWvnle1-hSEB7LUsMwpyLJD8QVfk130_assertion wasDerivedFrom befree-20150227 NP810494.RAv-iTy63E3kFjAWdhWvnle1-hSEB7LUsMwpyLJD8QVfk130_provenance.
- NP810494.RAv-iTy63E3kFjAWdhWvnle1-hSEB7LUsMwpyLJD8QVfk130_assertion wasGeneratedBy ECO_0000203 NP810494.RAv-iTy63E3kFjAWdhWvnle1-hSEB7LUsMwpyLJD8QVfk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP810494.RAv-iTy63E3kFjAWdhWvnle1-hSEB7LUsMwpyLJD8QVfk130_provenance.