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- source_evidence_literature type ECO_0000212 NP489501.RAXoj4TTt1bhV0fLGd2OhqC-eF-7H0PwwSqmw9fjk8o0U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP489501.RAXoj4TTt1bhV0fLGd2OhqC-eF-7H0PwwSqmw9fjk8o0U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP489501.RAXoj4TTt1bhV0fLGd2OhqC-eF-7H0PwwSqmw9fjk8o0U130_provenance.
- NP489501.RAXoj4TTt1bhV0fLGd2OhqC-eF-7H0PwwSqmw9fjk8o0U130_assertion description "[We previously reported that a deficient form of the C4B gene, termed the C4B null allele (no C4B protein produced) had an increased frequently in autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP489501.RAXoj4TTt1bhV0fLGd2OhqC-eF-7H0PwwSqmw9fjk8o0U130_provenance.
- NP489501.RAXoj4TTt1bhV0fLGd2OhqC-eF-7H0PwwSqmw9fjk8o0U130_assertion evidence source_evidence_literature NP489501.RAXoj4TTt1bhV0fLGd2OhqC-eF-7H0PwwSqmw9fjk8o0U130_provenance.
- NP489501.RAXoj4TTt1bhV0fLGd2OhqC-eF-7H0PwwSqmw9fjk8o0U130_assertion SIO_000772 8871944 NP489501.RAXoj4TTt1bhV0fLGd2OhqC-eF-7H0PwwSqmw9fjk8o0U130_provenance.
- NP489501.RAXoj4TTt1bhV0fLGd2OhqC-eF-7H0PwwSqmw9fjk8o0U130_assertion wasDerivedFrom befree-20140225 NP489501.RAXoj4TTt1bhV0fLGd2OhqC-eF-7H0PwwSqmw9fjk8o0U130_provenance.
- NP489501.RAXoj4TTt1bhV0fLGd2OhqC-eF-7H0PwwSqmw9fjk8o0U130_assertion wasGeneratedBy ECO_0000203 NP489501.RAXoj4TTt1bhV0fLGd2OhqC-eF-7H0PwwSqmw9fjk8o0U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP489501.RAXoj4TTt1bhV0fLGd2OhqC-eF-7H0PwwSqmw9fjk8o0U130_provenance.