Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_provenance.
- NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_assertion description "[This study demonstrates that ACE genotype frequencies are similar in index patients with VUR and their unaffected siblings, thus suggesting that the ACE gene is not involved in the development of familial VUR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_provenance.
- NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_assertion evidence source_evidence_literature NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_provenance.
- NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_assertion SIO_000772 11409168 NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_provenance.
- NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_assertion wasDerivedFrom befree-20140225 NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_provenance.
- NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_assertion wasGeneratedBy ECO_0000203 NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_provenance.