Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP718302.RAfH1VUnKG3Hb3MH8Sh4DcDQZTaiSu3fBWQyjG0nPvD3Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718302.RAfH1VUnKG3Hb3MH8Sh4DcDQZTaiSu3fBWQyjG0nPvD3Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718302.RAfH1VUnKG3Hb3MH8Sh4DcDQZTaiSu3fBWQyjG0nPvD3Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718302.RAfH1VUnKG3Hb3MH8Sh4DcDQZTaiSu3fBWQyjG0nPvD3Y130_provenance.
- NP718302.RAfH1VUnKG3Hb3MH8Sh4DcDQZTaiSu3fBWQyjG0nPvD3Y130_assertion description "[In a panel of 34 patients with isolated hypodontia, the candidate gene WNT10A and the genes MSX1, PAX9, IRF6 and AXIN2 have been sequenced.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718302.RAfH1VUnKG3Hb3MH8Sh4DcDQZTaiSu3fBWQyjG0nPvD3Y130_provenance.
- NP718302.RAfH1VUnKG3Hb3MH8Sh4DcDQZTaiSu3fBWQyjG0nPvD3Y130_assertion evidence source_evidence_literature NP718302.RAfH1VUnKG3Hb3MH8Sh4DcDQZTaiSu3fBWQyjG0nPvD3Y130_provenance.
- NP718302.RAfH1VUnKG3Hb3MH8Sh4DcDQZTaiSu3fBWQyjG0nPvD3Y130_assertion SIO_000772 22581971 NP718302.RAfH1VUnKG3Hb3MH8Sh4DcDQZTaiSu3fBWQyjG0nPvD3Y130_provenance.
- NP718302.RAfH1VUnKG3Hb3MH8Sh4DcDQZTaiSu3fBWQyjG0nPvD3Y130_assertion wasDerivedFrom befree-20140225 NP718302.RAfH1VUnKG3Hb3MH8Sh4DcDQZTaiSu3fBWQyjG0nPvD3Y130_provenance.
- NP718302.RAfH1VUnKG3Hb3MH8Sh4DcDQZTaiSu3fBWQyjG0nPvD3Y130_assertion wasGeneratedBy ECO_0000203 NP718302.RAfH1VUnKG3Hb3MH8Sh4DcDQZTaiSu3fBWQyjG0nPvD3Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP718302.RAfH1VUnKG3Hb3MH8Sh4DcDQZTaiSu3fBWQyjG0nPvD3Y130_provenance.