Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP609358.RATagRn4mJc74IDSsTPhVbjD2zvzdww3DfCyaiBgwFnho130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP609358.RATagRn4mJc74IDSsTPhVbjD2zvzdww3DfCyaiBgwFnho130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP609358.RATagRn4mJc74IDSsTPhVbjD2zvzdww3DfCyaiBgwFnho130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP609358.RATagRn4mJc74IDSsTPhVbjD2zvzdww3DfCyaiBgwFnho130_provenance.
- befree-20150227 importedOn "2015-02-27" NP609358.RATagRn4mJc74IDSsTPhVbjD2zvzdww3DfCyaiBgwFnho130_provenance.
- NP609358.RATagRn4mJc74IDSsTPhVbjD2zvzdww3DfCyaiBgwFnho130_assertion wasGeneratedBy ECO_0000203 NP609358.RATagRn4mJc74IDSsTPhVbjD2zvzdww3DfCyaiBgwFnho130_provenance.
- NP609358.RATagRn4mJc74IDSsTPhVbjD2zvzdww3DfCyaiBgwFnho130_assertion wasDerivedFrom befree-20150227 NP609358.RATagRn4mJc74IDSsTPhVbjD2zvzdww3DfCyaiBgwFnho130_provenance.
- NP609358.RATagRn4mJc74IDSsTPhVbjD2zvzdww3DfCyaiBgwFnho130_assertion SIO_000772 23539225 NP609358.RATagRn4mJc74IDSsTPhVbjD2zvzdww3DfCyaiBgwFnho130_provenance.
- NP609358.RATagRn4mJc74IDSsTPhVbjD2zvzdww3DfCyaiBgwFnho130_assertion evidence source_evidence_literature NP609358.RATagRn4mJc74IDSsTPhVbjD2zvzdww3DfCyaiBgwFnho130_provenance.
- NP609358.RATagRn4mJc74IDSsTPhVbjD2zvzdww3DfCyaiBgwFnho130_assertion description "[This study reports the screening of two genes (HNF1B and PAX2) involved in monogenic syndromic CAKUT in a cohort of 103 fetuses from 91 families with very severe CAKUT that appeared isolated by fetal ultrasound examination and led to termination of pregnancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609358.RATagRn4mJc74IDSsTPhVbjD2zvzdww3DfCyaiBgwFnho130_provenance.