Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP217667.RAcaWP7uMzQdu9nGte7cOvt2cP0rxZdMwR8SSnaEqCRX0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP217667.RAcaWP7uMzQdu9nGte7cOvt2cP0rxZdMwR8SSnaEqCRX0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP217667.RAcaWP7uMzQdu9nGte7cOvt2cP0rxZdMwR8SSnaEqCRX0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP217667.RAcaWP7uMzQdu9nGte7cOvt2cP0rxZdMwR8SSnaEqCRX0130_provenance.
- NP217667.RAcaWP7uMzQdu9nGte7cOvt2cP0rxZdMwR8SSnaEqCRX0130_assertion description "[Molecular genetics of hereditary thyroid diseases due to a defect in the thyroglobulin or thyroperoxidase synthesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217667.RAcaWP7uMzQdu9nGte7cOvt2cP0rxZdMwR8SSnaEqCRX0130_provenance.
- NP217667.RAcaWP7uMzQdu9nGte7cOvt2cP0rxZdMwR8SSnaEqCRX0130_assertion evidence source_evidence_literature NP217667.RAcaWP7uMzQdu9nGte7cOvt2cP0rxZdMwR8SSnaEqCRX0130_provenance.
- NP217667.RAcaWP7uMzQdu9nGte7cOvt2cP0rxZdMwR8SSnaEqCRX0130_assertion SIO_000772 7549998 NP217667.RAcaWP7uMzQdu9nGte7cOvt2cP0rxZdMwR8SSnaEqCRX0130_provenance.
- NP217667.RAcaWP7uMzQdu9nGte7cOvt2cP0rxZdMwR8SSnaEqCRX0130_assertion wasDerivedFrom befree-20140225 NP217667.RAcaWP7uMzQdu9nGte7cOvt2cP0rxZdMwR8SSnaEqCRX0130_provenance.
- NP217667.RAcaWP7uMzQdu9nGte7cOvt2cP0rxZdMwR8SSnaEqCRX0130_assertion wasGeneratedBy ECO_0000203 NP217667.RAcaWP7uMzQdu9nGte7cOvt2cP0rxZdMwR8SSnaEqCRX0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP217667.RAcaWP7uMzQdu9nGte7cOvt2cP0rxZdMwR8SSnaEqCRX0130_provenance.