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- source_evidence_literature type ECO_0000212 NP545054.RAUn3AZ3LCZpQBTpvXV1LVPjAalIJMMjkm1ZBilno6fb8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP545054.RAUn3AZ3LCZpQBTpvXV1LVPjAalIJMMjkm1ZBilno6fb8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP545054.RAUn3AZ3LCZpQBTpvXV1LVPjAalIJMMjkm1ZBilno6fb8130_provenance.
- NP545054.RAUn3AZ3LCZpQBTpvXV1LVPjAalIJMMjkm1ZBilno6fb8130_assertion description "[In recent years, through a variety of mouse mutants that carry multigene and single gene mutations, we have learned that mutation in a single gene, Tbx1, is responsible for most of the congenital defects seen in the mouse models and in patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP545054.RAUn3AZ3LCZpQBTpvXV1LVPjAalIJMMjkm1ZBilno6fb8130_provenance.
- NP545054.RAUn3AZ3LCZpQBTpvXV1LVPjAalIJMMjkm1ZBilno6fb8130_assertion evidence source_evidence_literature NP545054.RAUn3AZ3LCZpQBTpvXV1LVPjAalIJMMjkm1ZBilno6fb8130_provenance.
- NP545054.RAUn3AZ3LCZpQBTpvXV1LVPjAalIJMMjkm1ZBilno6fb8130_assertion SIO_000772 16616724 NP545054.RAUn3AZ3LCZpQBTpvXV1LVPjAalIJMMjkm1ZBilno6fb8130_provenance.
- NP545054.RAUn3AZ3LCZpQBTpvXV1LVPjAalIJMMjkm1ZBilno6fb8130_assertion wasDerivedFrom befree-2016 NP545054.RAUn3AZ3LCZpQBTpvXV1LVPjAalIJMMjkm1ZBilno6fb8130_provenance.
- NP545054.RAUn3AZ3LCZpQBTpvXV1LVPjAalIJMMjkm1ZBilno6fb8130_assertion wasGeneratedBy ECO_0000203 NP545054.RAUn3AZ3LCZpQBTpvXV1LVPjAalIJMMjkm1ZBilno6fb8130_provenance.
- befree-2016 importedOn "2016-02-19" NP545054.RAUn3AZ3LCZpQBTpvXV1LVPjAalIJMMjkm1ZBilno6fb8130_provenance.