Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP123484.RAYylNBZUzbPg_YoWKFd6AFTDb68O6NSPy9We-1Rb9xx4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP123484.RAYylNBZUzbPg_YoWKFd6AFTDb68O6NSPy9We-1Rb9xx4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP123484.RAYylNBZUzbPg_YoWKFd6AFTDb68O6NSPy9We-1Rb9xx4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP123484.RAYylNBZUzbPg_YoWKFd6AFTDb68O6NSPy9We-1Rb9xx4130_provenance.
- NP123484.RAYylNBZUzbPg_YoWKFd6AFTDb68O6NSPy9We-1Rb9xx4130_assertion description "[Statistical analysis of our entire data revealed significant differences in the distribution of ACVRL1 and ENG mutations among HHT patients with and without liver involvement (p = 0.0016).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP123484.RAYylNBZUzbPg_YoWKFd6AFTDb68O6NSPy9We-1Rb9xx4130_provenance.
- NP123484.RAYylNBZUzbPg_YoWKFd6AFTDb68O6NSPy9We-1Rb9xx4130_assertion evidence source_evidence_literature NP123484.RAYylNBZUzbPg_YoWKFd6AFTDb68O6NSPy9We-1Rb9xx4130_provenance.
- NP123484.RAYylNBZUzbPg_YoWKFd6AFTDb68O6NSPy9We-1Rb9xx4130_assertion SIO_000772 18498373 NP123484.RAYylNBZUzbPg_YoWKFd6AFTDb68O6NSPy9We-1Rb9xx4130_provenance.
- NP123484.RAYylNBZUzbPg_YoWKFd6AFTDb68O6NSPy9We-1Rb9xx4130_assertion wasDerivedFrom gad-20150221 NP123484.RAYylNBZUzbPg_YoWKFd6AFTDb68O6NSPy9We-1Rb9xx4130_provenance.
- NP123484.RAYylNBZUzbPg_YoWKFd6AFTDb68O6NSPy9We-1Rb9xx4130_assertion wasGeneratedBy ECO_0000203 NP123484.RAYylNBZUzbPg_YoWKFd6AFTDb68O6NSPy9We-1Rb9xx4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP123484.RAYylNBZUzbPg_YoWKFd6AFTDb68O6NSPy9We-1Rb9xx4130_provenance.