Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP215820.RANIBcDPmGtr2o_X0RCaSDt8L5vaypQC9fGu9x7qJI23c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP215820.RANIBcDPmGtr2o_X0RCaSDt8L5vaypQC9fGu9x7qJI23c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP215820.RANIBcDPmGtr2o_X0RCaSDt8L5vaypQC9fGu9x7qJI23c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP215820.RANIBcDPmGtr2o_X0RCaSDt8L5vaypQC9fGu9x7qJI23c130_provenance.
- NP215820.RANIBcDPmGtr2o_X0RCaSDt8L5vaypQC9fGu9x7qJI23c130_assertion description "[Mutation analysis in ENG and ACVRL1 genes was performed in hereditary hemorrhagic telangiectasia patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215820.RANIBcDPmGtr2o_X0RCaSDt8L5vaypQC9fGu9x7qJI23c130_provenance.
- NP215820.RANIBcDPmGtr2o_X0RCaSDt8L5vaypQC9fGu9x7qJI23c130_assertion evidence source_evidence_literature NP215820.RANIBcDPmGtr2o_X0RCaSDt8L5vaypQC9fGu9x7qJI23c130_provenance.
- NP215820.RANIBcDPmGtr2o_X0RCaSDt8L5vaypQC9fGu9x7qJI23c130_assertion SIO_000772 17786384 NP215820.RANIBcDPmGtr2o_X0RCaSDt8L5vaypQC9fGu9x7qJI23c130_provenance.
- NP215820.RANIBcDPmGtr2o_X0RCaSDt8L5vaypQC9fGu9x7qJI23c130_assertion wasDerivedFrom lhgdn-20090331 NP215820.RANIBcDPmGtr2o_X0RCaSDt8L5vaypQC9fGu9x7qJI23c130_provenance.
- NP215820.RANIBcDPmGtr2o_X0RCaSDt8L5vaypQC9fGu9x7qJI23c130_assertion wasGeneratedBy ECO_0000203 NP215820.RANIBcDPmGtr2o_X0RCaSDt8L5vaypQC9fGu9x7qJI23c130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP215820.RANIBcDPmGtr2o_X0RCaSDt8L5vaypQC9fGu9x7qJI23c130_provenance.