Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1102134.RAvFkhflv8epwa8hHPPScd-2o7t9dDbhIbGqOChg3gycI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1102134.RAvFkhflv8epwa8hHPPScd-2o7t9dDbhIbGqOChg3gycI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1102134.RAvFkhflv8epwa8hHPPScd-2o7t9dDbhIbGqOChg3gycI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1102134.RAvFkhflv8epwa8hHPPScd-2o7t9dDbhIbGqOChg3gycI130_provenance.
- NP1102134.RAvFkhflv8epwa8hHPPScd-2o7t9dDbhIbGqOChg3gycI130_assertion description "[The phenotype was consistent with previous descriptions of AOA2, except for a higher frequency of strabism, and for the absence of oculomotor apraxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1102134.RAvFkhflv8epwa8hHPPScd-2o7t9dDbhIbGqOChg3gycI130_provenance.
- NP1102134.RAvFkhflv8epwa8hHPPScd-2o7t9dDbhIbGqOChg3gycI130_assertion evidence source_evidence_literature NP1102134.RAvFkhflv8epwa8hHPPScd-2o7t9dDbhIbGqOChg3gycI130_provenance.
- NP1102134.RAvFkhflv8epwa8hHPPScd-2o7t9dDbhIbGqOChg3gycI130_assertion SIO_000772 23941260 NP1102134.RAvFkhflv8epwa8hHPPScd-2o7t9dDbhIbGqOChg3gycI130_provenance.
- NP1102134.RAvFkhflv8epwa8hHPPScd-2o7t9dDbhIbGqOChg3gycI130_assertion wasDerivedFrom befree-2016 NP1102134.RAvFkhflv8epwa8hHPPScd-2o7t9dDbhIbGqOChg3gycI130_provenance.
- NP1102134.RAvFkhflv8epwa8hHPPScd-2o7t9dDbhIbGqOChg3gycI130_assertion wasGeneratedBy ECO_0000203 NP1102134.RAvFkhflv8epwa8hHPPScd-2o7t9dDbhIbGqOChg3gycI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1102134.RAvFkhflv8epwa8hHPPScd-2o7t9dDbhIbGqOChg3gycI130_provenance.