Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP583339.RAXn8glMsuAxo-KIY2ED4mqYSv9sxDo_mPCoAgVTX55vc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP583339.RAXn8glMsuAxo-KIY2ED4mqYSv9sxDo_mPCoAgVTX55vc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP583339.RAXn8glMsuAxo-KIY2ED4mqYSv9sxDo_mPCoAgVTX55vc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP583339.RAXn8glMsuAxo-KIY2ED4mqYSv9sxDo_mPCoAgVTX55vc130_provenance.
- NP583339.RAXn8glMsuAxo-KIY2ED4mqYSv9sxDo_mPCoAgVTX55vc130_assertion description "[Longitudinal follow-up revealed that this family has X-linked heterotaxy due to a missense mutation, c.1048A>G(R350G), in the third zinc finger domain of ZIC3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583339.RAXn8glMsuAxo-KIY2ED4mqYSv9sxDo_mPCoAgVTX55vc130_provenance.
- NP583339.RAXn8glMsuAxo-KIY2ED4mqYSv9sxDo_mPCoAgVTX55vc130_assertion evidence source_evidence_literature NP583339.RAXn8glMsuAxo-KIY2ED4mqYSv9sxDo_mPCoAgVTX55vc130_provenance.
- NP583339.RAXn8glMsuAxo-KIY2ED4mqYSv9sxDo_mPCoAgVTX55vc130_assertion SIO_000772 22171628 NP583339.RAXn8glMsuAxo-KIY2ED4mqYSv9sxDo_mPCoAgVTX55vc130_provenance.
- NP583339.RAXn8glMsuAxo-KIY2ED4mqYSv9sxDo_mPCoAgVTX55vc130_assertion wasDerivedFrom befree-20140225 NP583339.RAXn8glMsuAxo-KIY2ED4mqYSv9sxDo_mPCoAgVTX55vc130_provenance.
- NP583339.RAXn8glMsuAxo-KIY2ED4mqYSv9sxDo_mPCoAgVTX55vc130_assertion wasGeneratedBy ECO_0000203 NP583339.RAXn8glMsuAxo-KIY2ED4mqYSv9sxDo_mPCoAgVTX55vc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP583339.RAXn8glMsuAxo-KIY2ED4mqYSv9sxDo_mPCoAgVTX55vc130_provenance.