Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP514487.RAaVbN_HEebDdMrxYcLOqlFsCoy-VV2NSQkmm60KxVXSM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP514487.RAaVbN_HEebDdMrxYcLOqlFsCoy-VV2NSQkmm60KxVXSM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP514487.RAaVbN_HEebDdMrxYcLOqlFsCoy-VV2NSQkmm60KxVXSM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP514487.RAaVbN_HEebDdMrxYcLOqlFsCoy-VV2NSQkmm60KxVXSM130_provenance.
- NP514487.RAaVbN_HEebDdMrxYcLOqlFsCoy-VV2NSQkmm60KxVXSM130_assertion description "[To estimate the frequency of JAG1 mutations in cases with right-sided cardiac defects not otherwise diagnosed with AGS, we screened 94 cases with tetralogy of Fallot (TOF) and 50 with pulmonic stenosis/peripheral pulmonary stenosis (PS/PPS) or pulmonary valve atresia with intact ventricular septum (PA) for mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP514487.RAaVbN_HEebDdMrxYcLOqlFsCoy-VV2NSQkmm60KxVXSM130_provenance.
- NP514487.RAaVbN_HEebDdMrxYcLOqlFsCoy-VV2NSQkmm60KxVXSM130_assertion evidence source_evidence_literature NP514487.RAaVbN_HEebDdMrxYcLOqlFsCoy-VV2NSQkmm60KxVXSM130_provenance.
- NP514487.RAaVbN_HEebDdMrxYcLOqlFsCoy-VV2NSQkmm60KxVXSM130_assertion SIO_000772 20437614 NP514487.RAaVbN_HEebDdMrxYcLOqlFsCoy-VV2NSQkmm60KxVXSM130_provenance.
- NP514487.RAaVbN_HEebDdMrxYcLOqlFsCoy-VV2NSQkmm60KxVXSM130_assertion wasDerivedFrom befree-20140225 NP514487.RAaVbN_HEebDdMrxYcLOqlFsCoy-VV2NSQkmm60KxVXSM130_provenance.
- NP514487.RAaVbN_HEebDdMrxYcLOqlFsCoy-VV2NSQkmm60KxVXSM130_assertion wasGeneratedBy ECO_0000203 NP514487.RAaVbN_HEebDdMrxYcLOqlFsCoy-VV2NSQkmm60KxVXSM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP514487.RAaVbN_HEebDdMrxYcLOqlFsCoy-VV2NSQkmm60KxVXSM130_provenance.