Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP343368.RAcHLnV_lGNadVx-c64mvRKKfNbXo4-QYR8t068QR27Bs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP343368.RAcHLnV_lGNadVx-c64mvRKKfNbXo4-QYR8t068QR27Bs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP343368.RAcHLnV_lGNadVx-c64mvRKKfNbXo4-QYR8t068QR27Bs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP343368.RAcHLnV_lGNadVx-c64mvRKKfNbXo4-QYR8t068QR27Bs130_provenance.
- befree-2016 importedOn "2016-02-19" NP343368.RAcHLnV_lGNadVx-c64mvRKKfNbXo4-QYR8t068QR27Bs130_provenance.
- NP343368.RAcHLnV_lGNadVx-c64mvRKKfNbXo4-QYR8t068QR27Bs130_assertion wasGeneratedBy ECO_0000203 NP343368.RAcHLnV_lGNadVx-c64mvRKKfNbXo4-QYR8t068QR27Bs130_provenance.
- NP343368.RAcHLnV_lGNadVx-c64mvRKKfNbXo4-QYR8t068QR27Bs130_assertion wasDerivedFrom befree-2016 NP343368.RAcHLnV_lGNadVx-c64mvRKKfNbXo4-QYR8t068QR27Bs130_provenance.
- NP343368.RAcHLnV_lGNadVx-c64mvRKKfNbXo4-QYR8t068QR27Bs130_assertion SIO_000772 11812941 NP343368.RAcHLnV_lGNadVx-c64mvRKKfNbXo4-QYR8t068QR27Bs130_provenance.
- NP343368.RAcHLnV_lGNadVx-c64mvRKKfNbXo4-QYR8t068QR27Bs130_assertion evidence source_evidence_literature NP343368.RAcHLnV_lGNadVx-c64mvRKKfNbXo4-QYR8t068QR27Bs130_provenance.
- NP343368.RAcHLnV_lGNadVx-c64mvRKKfNbXo4-QYR8t068QR27Bs130_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." NP343368.RAcHLnV_lGNadVx-c64mvRKKfNbXo4-QYR8t068QR27Bs130_provenance.