Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP643264.RAgTh7RK1tVvXv9pGtVF7xXy6cFxUaZFy2va5ugvgCc6A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP643264.RAgTh7RK1tVvXv9pGtVF7xXy6cFxUaZFy2va5ugvgCc6A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP643264.RAgTh7RK1tVvXv9pGtVF7xXy6cFxUaZFy2va5ugvgCc6A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP643264.RAgTh7RK1tVvXv9pGtVF7xXy6cFxUaZFy2va5ugvgCc6A130_provenance.
- NP643264.RAgTh7RK1tVvXv9pGtVF7xXy6cFxUaZFy2va5ugvgCc6A130_assertion description "[Recently, a deletion mutation disrupting both TSC2 and PKD1 has been described in young children with tuberous sclerosis complex with severe renal cystic disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP643264.RAgTh7RK1tVvXv9pGtVF7xXy6cFxUaZFy2va5ugvgCc6A130_provenance.
- NP643264.RAgTh7RK1tVvXv9pGtVF7xXy6cFxUaZFy2va5ugvgCc6A130_assertion evidence source_evidence_literature NP643264.RAgTh7RK1tVvXv9pGtVF7xXy6cFxUaZFy2va5ugvgCc6A130_provenance.
- NP643264.RAgTh7RK1tVvXv9pGtVF7xXy6cFxUaZFy2va5ugvgCc6A130_assertion SIO_000772 11812941 NP643264.RAgTh7RK1tVvXv9pGtVF7xXy6cFxUaZFy2va5ugvgCc6A130_provenance.
- NP643264.RAgTh7RK1tVvXv9pGtVF7xXy6cFxUaZFy2va5ugvgCc6A130_assertion wasDerivedFrom befree-20150227 NP643264.RAgTh7RK1tVvXv9pGtVF7xXy6cFxUaZFy2va5ugvgCc6A130_provenance.
- NP643264.RAgTh7RK1tVvXv9pGtVF7xXy6cFxUaZFy2va5ugvgCc6A130_assertion wasGeneratedBy ECO_0000203 NP643264.RAgTh7RK1tVvXv9pGtVF7xXy6cFxUaZFy2va5ugvgCc6A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP643264.RAgTh7RK1tVvXv9pGtVF7xXy6cFxUaZFy2va5ugvgCc6A130_provenance.