Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP673863.RAwX9bnUtcucJ3eOJOIz3Czp0KpU3eSPTjo0UOm_6JQgo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP673863.RAwX9bnUtcucJ3eOJOIz3Czp0KpU3eSPTjo0UOm_6JQgo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP673863.RAwX9bnUtcucJ3eOJOIz3Czp0KpU3eSPTjo0UOm_6JQgo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP673863.RAwX9bnUtcucJ3eOJOIz3Czp0KpU3eSPTjo0UOm_6JQgo130_provenance.
- NP673863.RAwX9bnUtcucJ3eOJOIz3Czp0KpU3eSPTjo0UOm_6JQgo130_assertion description "[Common genetic variants in four genes (GREM1, EYA1, ROBO2 and UPK3A) show a trend towards association with the development of primary VUR (GREM1, EYA1, ROBO2) or duplex collecting system (EYA1 and UPK3A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP673863.RAwX9bnUtcucJ3eOJOIz3Czp0KpU3eSPTjo0UOm_6JQgo130_provenance.
- NP673863.RAwX9bnUtcucJ3eOJOIz3Czp0KpU3eSPTjo0UOm_6JQgo130_assertion evidence source_evidence_literature NP673863.RAwX9bnUtcucJ3eOJOIz3Czp0KpU3eSPTjo0UOm_6JQgo130_provenance.
- NP673863.RAwX9bnUtcucJ3eOJOIz3Czp0KpU3eSPTjo0UOm_6JQgo130_assertion SIO_000772 22558067 NP673863.RAwX9bnUtcucJ3eOJOIz3Czp0KpU3eSPTjo0UOm_6JQgo130_provenance.
- NP673863.RAwX9bnUtcucJ3eOJOIz3Czp0KpU3eSPTjo0UOm_6JQgo130_assertion wasDerivedFrom befree-20150227 NP673863.RAwX9bnUtcucJ3eOJOIz3Czp0KpU3eSPTjo0UOm_6JQgo130_provenance.
- NP673863.RAwX9bnUtcucJ3eOJOIz3Czp0KpU3eSPTjo0UOm_6JQgo130_assertion wasGeneratedBy ECO_0000203 NP673863.RAwX9bnUtcucJ3eOJOIz3Czp0KpU3eSPTjo0UOm_6JQgo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP673863.RAwX9bnUtcucJ3eOJOIz3Czp0KpU3eSPTjo0UOm_6JQgo130_provenance.