Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP940672.RAPWGwkSrHHctETW_uaVTMpuQS_HL7rQZx6Tztqxj7DqM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP940672.RAPWGwkSrHHctETW_uaVTMpuQS_HL7rQZx6Tztqxj7DqM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP940672.RAPWGwkSrHHctETW_uaVTMpuQS_HL7rQZx6Tztqxj7DqM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP940672.RAPWGwkSrHHctETW_uaVTMpuQS_HL7rQZx6Tztqxj7DqM130_provenance.
- NP940672.RAPWGwkSrHHctETW_uaVTMpuQS_HL7rQZx6Tztqxj7DqM130_assertion description "[All four siblings from family 1 had shorter axial biometry (ACD range 2.06-2.74 mm; AL range 20.46-22.60 mm) than the normal population, contributing to their risk of ACG development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP940672.RAPWGwkSrHHctETW_uaVTMpuQS_HL7rQZx6Tztqxj7DqM130_provenance.
- NP940672.RAPWGwkSrHHctETW_uaVTMpuQS_HL7rQZx6Tztqxj7DqM130_assertion evidence source_evidence_literature NP940672.RAPWGwkSrHHctETW_uaVTMpuQS_HL7rQZx6Tztqxj7DqM130_provenance.
- NP940672.RAPWGwkSrHHctETW_uaVTMpuQS_HL7rQZx6Tztqxj7DqM130_assertion SIO_000772 21921978 NP940672.RAPWGwkSrHHctETW_uaVTMpuQS_HL7rQZx6Tztqxj7DqM130_provenance.
- NP940672.RAPWGwkSrHHctETW_uaVTMpuQS_HL7rQZx6Tztqxj7DqM130_assertion wasDerivedFrom befree-20150227 NP940672.RAPWGwkSrHHctETW_uaVTMpuQS_HL7rQZx6Tztqxj7DqM130_provenance.
- NP940672.RAPWGwkSrHHctETW_uaVTMpuQS_HL7rQZx6Tztqxj7DqM130_assertion wasGeneratedBy ECO_0000203 NP940672.RAPWGwkSrHHctETW_uaVTMpuQS_HL7rQZx6Tztqxj7DqM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP940672.RAPWGwkSrHHctETW_uaVTMpuQS_HL7rQZx6Tztqxj7DqM130_provenance.