Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP18737.RACFb-sONApPHPswvmtiFnRhL-fYeKZ0KJPPd7upMbtJA130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP18737.RACFb-sONApPHPswvmtiFnRhL-fYeKZ0KJPPd7upMbtJA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP18737.RACFb-sONApPHPswvmtiFnRhL-fYeKZ0KJPPd7upMbtJA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP18737.RACFb-sONApPHPswvmtiFnRhL-fYeKZ0KJPPd7upMbtJA130_provenance.
- NP18737.RACFb-sONApPHPswvmtiFnRhL-fYeKZ0KJPPd7upMbtJA130_assertion description "[Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP18737.RACFb-sONApPHPswvmtiFnRhL-fYeKZ0KJPPd7upMbtJA130_provenance.
- NP18737.RACFb-sONApPHPswvmtiFnRhL-fYeKZ0KJPPd7upMbtJA130_assertion evidence source_evidence_curated NP18737.RACFb-sONApPHPswvmtiFnRhL-fYeKZ0KJPPd7upMbtJA130_provenance.
- NP18737.RACFb-sONApPHPswvmtiFnRhL-fYeKZ0KJPPd7upMbtJA130_assertion SIO_000772 19029900 NP18737.RACFb-sONApPHPswvmtiFnRhL-fYeKZ0KJPPd7upMbtJA130_provenance.
- NP18737.RACFb-sONApPHPswvmtiFnRhL-fYeKZ0KJPPd7upMbtJA130_assertion wasDerivedFrom ctd_human-20130708 NP18737.RACFb-sONApPHPswvmtiFnRhL-fYeKZ0KJPPd7upMbtJA130_provenance.
- NP18737.RACFb-sONApPHPswvmtiFnRhL-fYeKZ0KJPPd7upMbtJA130_assertion wasGeneratedBy ECO_0000218 NP18737.RACFb-sONApPHPswvmtiFnRhL-fYeKZ0KJPPd7upMbtJA130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP18737.RACFb-sONApPHPswvmtiFnRhL-fYeKZ0KJPPd7upMbtJA130_provenance.