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- source_evidence_literature type ECO_0000212 NP735695.RAxKVa9x0WczGnPS0Zgeol-T3l48ONEdAJR-I1tRuwx7A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP735695.RAxKVa9x0WczGnPS0Zgeol-T3l48ONEdAJR-I1tRuwx7A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP735695.RAxKVa9x0WczGnPS0Zgeol-T3l48ONEdAJR-I1tRuwx7A130_provenance.
- NP735695.RAxKVa9x0WczGnPS0Zgeol-T3l48ONEdAJR-I1tRuwx7A130_assertion description "[Identification and characterization of mutations in FANCL gene: a second case of Fanconi anemia belonging to FA-L complementation group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP735695.RAxKVa9x0WczGnPS0Zgeol-T3l48ONEdAJR-I1tRuwx7A130_provenance.
- NP735695.RAxKVa9x0WczGnPS0Zgeol-T3l48ONEdAJR-I1tRuwx7A130_assertion evidence source_evidence_literature NP735695.RAxKVa9x0WczGnPS0Zgeol-T3l48ONEdAJR-I1tRuwx7A130_provenance.
- NP735695.RAxKVa9x0WczGnPS0Zgeol-T3l48ONEdAJR-I1tRuwx7A130_assertion SIO_000772 19405097 NP735695.RAxKVa9x0WczGnPS0Zgeol-T3l48ONEdAJR-I1tRuwx7A130_provenance.
- NP735695.RAxKVa9x0WczGnPS0Zgeol-T3l48ONEdAJR-I1tRuwx7A130_assertion wasDerivedFrom befree-2016 NP735695.RAxKVa9x0WczGnPS0Zgeol-T3l48ONEdAJR-I1tRuwx7A130_provenance.
- NP735695.RAxKVa9x0WczGnPS0Zgeol-T3l48ONEdAJR-I1tRuwx7A130_assertion wasGeneratedBy ECO_0000203 NP735695.RAxKVa9x0WczGnPS0Zgeol-T3l48ONEdAJR-I1tRuwx7A130_provenance.
- befree-2016 importedOn "2016-02-19" NP735695.RAxKVa9x0WczGnPS0Zgeol-T3l48ONEdAJR-I1tRuwx7A130_provenance.