Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP456342.RAJZnKFvtis5G6GkF4cW6PXlHPIvx2VPB8fBSYei2WG3g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP456342.RAJZnKFvtis5G6GkF4cW6PXlHPIvx2VPB8fBSYei2WG3g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP456342.RAJZnKFvtis5G6GkF4cW6PXlHPIvx2VPB8fBSYei2WG3g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP456342.RAJZnKFvtis5G6GkF4cW6PXlHPIvx2VPB8fBSYei2WG3g130_provenance.
- NP456342.RAJZnKFvtis5G6GkF4cW6PXlHPIvx2VPB8fBSYei2WG3g130_assertion description "[These results imply distinct molecular mechanisms for monosomy 7 and trisomy 8 MDS and implicate specific pathogenic pathways.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP456342.RAJZnKFvtis5G6GkF4cW6PXlHPIvx2VPB8fBSYei2WG3g130_provenance.
- NP456342.RAJZnKFvtis5G6GkF4cW6PXlHPIvx2VPB8fBSYei2WG3g130_assertion evidence source_evidence_literature NP456342.RAJZnKFvtis5G6GkF4cW6PXlHPIvx2VPB8fBSYei2WG3g130_provenance.
- NP456342.RAJZnKFvtis5G6GkF4cW6PXlHPIvx2VPB8fBSYei2WG3g130_assertion SIO_000772 15315976 NP456342.RAJZnKFvtis5G6GkF4cW6PXlHPIvx2VPB8fBSYei2WG3g130_provenance.
- NP456342.RAJZnKFvtis5G6GkF4cW6PXlHPIvx2VPB8fBSYei2WG3g130_assertion wasDerivedFrom befree-2016 NP456342.RAJZnKFvtis5G6GkF4cW6PXlHPIvx2VPB8fBSYei2WG3g130_provenance.
- NP456342.RAJZnKFvtis5G6GkF4cW6PXlHPIvx2VPB8fBSYei2WG3g130_assertion wasGeneratedBy ECO_0000203 NP456342.RAJZnKFvtis5G6GkF4cW6PXlHPIvx2VPB8fBSYei2WG3g130_provenance.
- befree-2016 importedOn "2016-02-19" NP456342.RAJZnKFvtis5G6GkF4cW6PXlHPIvx2VPB8fBSYei2WG3g130_provenance.