Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP149713.RAtiNPC3gPPG__Q_VTLBneTcYUPtxwsSFEElVrnkQVsBY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP149713.RAtiNPC3gPPG__Q_VTLBneTcYUPtxwsSFEElVrnkQVsBY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP149713.RAtiNPC3gPPG__Q_VTLBneTcYUPtxwsSFEElVrnkQVsBY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP149713.RAtiNPC3gPPG__Q_VTLBneTcYUPtxwsSFEElVrnkQVsBY130_provenance.
- NP149713.RAtiNPC3gPPG__Q_VTLBneTcYUPtxwsSFEElVrnkQVsBY130_assertion description "[Bi-allelic germline mutations of the Fanconi anemia (FA) genes, PALB2/FANCN and BRCA2/FANCD1, have been reported in a few Wilms tumor (WT) patients with an atypical FA phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149713.RAtiNPC3gPPG__Q_VTLBneTcYUPtxwsSFEElVrnkQVsBY130_provenance.
- NP149713.RAtiNPC3gPPG__Q_VTLBneTcYUPtxwsSFEElVrnkQVsBY130_assertion evidence source_evidence_literature NP149713.RAtiNPC3gPPG__Q_VTLBneTcYUPtxwsSFEElVrnkQVsBY130_provenance.
- NP149713.RAtiNPC3gPPG__Q_VTLBneTcYUPtxwsSFEElVrnkQVsBY130_assertion SIO_000772 20589654 NP149713.RAtiNPC3gPPG__Q_VTLBneTcYUPtxwsSFEElVrnkQVsBY130_provenance.
- NP149713.RAtiNPC3gPPG__Q_VTLBneTcYUPtxwsSFEElVrnkQVsBY130_assertion wasDerivedFrom gad-20150221 NP149713.RAtiNPC3gPPG__Q_VTLBneTcYUPtxwsSFEElVrnkQVsBY130_provenance.
- NP149713.RAtiNPC3gPPG__Q_VTLBneTcYUPtxwsSFEElVrnkQVsBY130_assertion wasGeneratedBy ECO_0000203 NP149713.RAtiNPC3gPPG__Q_VTLBneTcYUPtxwsSFEElVrnkQVsBY130_provenance.
- gad-20150221 importedOn "2015-02-21" NP149713.RAtiNPC3gPPG__Q_VTLBneTcYUPtxwsSFEElVrnkQVsBY130_provenance.