Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_provenance.
- NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_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." NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_provenance.
- NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_assertion evidence source_evidence_literature NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_provenance.
- NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_assertion SIO_000772 22171628 NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_provenance.
- NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_assertion wasDerivedFrom befree-20140225 NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_provenance.
- NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_assertion wasGeneratedBy ECO_0000203 NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP487135.RAqMVMm6BUqsT_WqXm5sqdZdKCKZCC5L3qRorBksxotNo130_provenance.