Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP206708.RAgPU7P_EfHqu4yop1N-48j6CxNIIC23xGslvUy4Wdc3o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP206708.RAgPU7P_EfHqu4yop1N-48j6CxNIIC23xGslvUy4Wdc3o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP206708.RAgPU7P_EfHqu4yop1N-48j6CxNIIC23xGslvUy4Wdc3o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP206708.RAgPU7P_EfHqu4yop1N-48j6CxNIIC23xGslvUy4Wdc3o130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP206708.RAgPU7P_EfHqu4yop1N-48j6CxNIIC23xGslvUy4Wdc3o130_provenance.
- NP206708.RAgPU7P_EfHqu4yop1N-48j6CxNIIC23xGslvUy4Wdc3o130_assertion wasGeneratedBy ECO_0000203 NP206708.RAgPU7P_EfHqu4yop1N-48j6CxNIIC23xGslvUy4Wdc3o130_provenance.
- NP206708.RAgPU7P_EfHqu4yop1N-48j6CxNIIC23xGslvUy4Wdc3o130_assertion wasDerivedFrom lhgdn-20090331 NP206708.RAgPU7P_EfHqu4yop1N-48j6CxNIIC23xGslvUy4Wdc3o130_provenance.
- NP206708.RAgPU7P_EfHqu4yop1N-48j6CxNIIC23xGslvUy4Wdc3o130_assertion SIO_000772 16007086 NP206708.RAgPU7P_EfHqu4yop1N-48j6CxNIIC23xGslvUy4Wdc3o130_provenance.
- NP206708.RAgPU7P_EfHqu4yop1N-48j6CxNIIC23xGslvUy4Wdc3o130_assertion evidence source_evidence_literature NP206708.RAgPU7P_EfHqu4yop1N-48j6CxNIIC23xGslvUy4Wdc3o130_provenance.
- NP206708.RAgPU7P_EfHqu4yop1N-48j6CxNIIC23xGslvUy4Wdc3o130_assertion description "[4 of 19 unrelated individuals with common variable immunodeficiency and 1 of 16 individuals with IgA deficiency had a missense mutation in one allele of TNFRSF13B]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206708.RAgPU7P_EfHqu4yop1N-48j6CxNIIC23xGslvUy4Wdc3o130_provenance.