Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP589787.RAfHP0vcA4Yb-48-qXniPVY1IMxnin0APSIQPCXeKXQFc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP589787.RAfHP0vcA4Yb-48-qXniPVY1IMxnin0APSIQPCXeKXQFc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP589787.RAfHP0vcA4Yb-48-qXniPVY1IMxnin0APSIQPCXeKXQFc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP589787.RAfHP0vcA4Yb-48-qXniPVY1IMxnin0APSIQPCXeKXQFc130_provenance.
- NP589787.RAfHP0vcA4Yb-48-qXniPVY1IMxnin0APSIQPCXeKXQFc130_assertion description "[Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency..]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP589787.RAfHP0vcA4Yb-48-qXniPVY1IMxnin0APSIQPCXeKXQFc130_provenance.
- NP589787.RAfHP0vcA4Yb-48-qXniPVY1IMxnin0APSIQPCXeKXQFc130_assertion evidence source_evidence_literature NP589787.RAfHP0vcA4Yb-48-qXniPVY1IMxnin0APSIQPCXeKXQFc130_provenance.
- NP589787.RAfHP0vcA4Yb-48-qXniPVY1IMxnin0APSIQPCXeKXQFc130_assertion SIO_000772 10852374 NP589787.RAfHP0vcA4Yb-48-qXniPVY1IMxnin0APSIQPCXeKXQFc130_provenance.
- NP589787.RAfHP0vcA4Yb-48-qXniPVY1IMxnin0APSIQPCXeKXQFc130_assertion wasDerivedFrom befree-20140225 NP589787.RAfHP0vcA4Yb-48-qXniPVY1IMxnin0APSIQPCXeKXQFc130_provenance.
- NP589787.RAfHP0vcA4Yb-48-qXniPVY1IMxnin0APSIQPCXeKXQFc130_assertion wasGeneratedBy ECO_0000203 NP589787.RAfHP0vcA4Yb-48-qXniPVY1IMxnin0APSIQPCXeKXQFc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP589787.RAfHP0vcA4Yb-48-qXniPVY1IMxnin0APSIQPCXeKXQFc130_provenance.