Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP961433.RAWf3BwP_CpBUFwzn3rXlnQPZtByVz5UQqnmYctiCiF28130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP961433.RAWf3BwP_CpBUFwzn3rXlnQPZtByVz5UQqnmYctiCiF28130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP961433.RAWf3BwP_CpBUFwzn3rXlnQPZtByVz5UQqnmYctiCiF28130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP961433.RAWf3BwP_CpBUFwzn3rXlnQPZtByVz5UQqnmYctiCiF28130_provenance.
- NP961433.RAWf3BwP_CpBUFwzn3rXlnQPZtByVz5UQqnmYctiCiF28130_assertion description "[Here, we present next-generation sequencing of all coding exons in the FCD2 critical interval in a multigenerational pedigree in which FCD segregates as an autosomal-dominant trait.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP961433.RAWf3BwP_CpBUFwzn3rXlnQPZtByVz5UQqnmYctiCiF28130_provenance.
- NP961433.RAWf3BwP_CpBUFwzn3rXlnQPZtByVz5UQqnmYctiCiF28130_assertion evidence source_evidence_literature NP961433.RAWf3BwP_CpBUFwzn3rXlnQPZtByVz5UQqnmYctiCiF28130_provenance.
- NP961433.RAWf3BwP_CpBUFwzn3rXlnQPZtByVz5UQqnmYctiCiF28130_assertion SIO_000772 22341973 NP961433.RAWf3BwP_CpBUFwzn3rXlnQPZtByVz5UQqnmYctiCiF28130_provenance.
- NP961433.RAWf3BwP_CpBUFwzn3rXlnQPZtByVz5UQqnmYctiCiF28130_assertion wasDerivedFrom befree-2016 NP961433.RAWf3BwP_CpBUFwzn3rXlnQPZtByVz5UQqnmYctiCiF28130_provenance.
- NP961433.RAWf3BwP_CpBUFwzn3rXlnQPZtByVz5UQqnmYctiCiF28130_assertion wasGeneratedBy ECO_0000203 NP961433.RAWf3BwP_CpBUFwzn3rXlnQPZtByVz5UQqnmYctiCiF28130_provenance.
- befree-2016 importedOn "2016-02-19" NP961433.RAWf3BwP_CpBUFwzn3rXlnQPZtByVz5UQqnmYctiCiF28130_provenance.