Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1113605.RABoGiJuKTjbNv5z3OOL6TMQX1vxzIRlLMbmmxaC1nevA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1113605.RABoGiJuKTjbNv5z3OOL6TMQX1vxzIRlLMbmmxaC1nevA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1113605.RABoGiJuKTjbNv5z3OOL6TMQX1vxzIRlLMbmmxaC1nevA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1113605.RABoGiJuKTjbNv5z3OOL6TMQX1vxzIRlLMbmmxaC1nevA130_provenance.
- NP1113605.RABoGiJuKTjbNv5z3OOL6TMQX1vxzIRlLMbmmxaC1nevA130_assertion description "[Germline mutations in RECQL4 and p53 lead to cancer predisposition syndromes, Rothmund-Thomson syndrome (RTS) and Li-Fraumeni syndrome (LFS), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1113605.RABoGiJuKTjbNv5z3OOL6TMQX1vxzIRlLMbmmxaC1nevA130_provenance.
- NP1113605.RABoGiJuKTjbNv5z3OOL6TMQX1vxzIRlLMbmmxaC1nevA130_assertion evidence source_evidence_literature NP1113605.RABoGiJuKTjbNv5z3OOL6TMQX1vxzIRlLMbmmxaC1nevA130_provenance.
- NP1113605.RABoGiJuKTjbNv5z3OOL6TMQX1vxzIRlLMbmmxaC1nevA130_assertion SIO_000772 24067899 NP1113605.RABoGiJuKTjbNv5z3OOL6TMQX1vxzIRlLMbmmxaC1nevA130_provenance.
- NP1113605.RABoGiJuKTjbNv5z3OOL6TMQX1vxzIRlLMbmmxaC1nevA130_assertion wasDerivedFrom befree-2016 NP1113605.RABoGiJuKTjbNv5z3OOL6TMQX1vxzIRlLMbmmxaC1nevA130_provenance.
- NP1113605.RABoGiJuKTjbNv5z3OOL6TMQX1vxzIRlLMbmmxaC1nevA130_assertion wasGeneratedBy ECO_0000203 NP1113605.RABoGiJuKTjbNv5z3OOL6TMQX1vxzIRlLMbmmxaC1nevA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1113605.RABoGiJuKTjbNv5z3OOL6TMQX1vxzIRlLMbmmxaC1nevA130_provenance.