Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP740604.RAGMKFBEhtvVtbWUxTOtG8gjBtiaN07EcfQBZESAo_TQY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP740604.RAGMKFBEhtvVtbWUxTOtG8gjBtiaN07EcfQBZESAo_TQY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP740604.RAGMKFBEhtvVtbWUxTOtG8gjBtiaN07EcfQBZESAo_TQY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP740604.RAGMKFBEhtvVtbWUxTOtG8gjBtiaN07EcfQBZESAo_TQY130_provenance.
- NP740604.RAGMKFBEhtvVtbWUxTOtG8gjBtiaN07EcfQBZESAo_TQY130_assertion description "[Here we describe the construction and characterization of DNA libraries for the Langer-Giedion syndrome chromosome region (LGCR, 8q23-24.1), Wilms tumor chromosome region 1 (WT1, 11p13), Prader-Willi syndrome/Angelman syndrome chromosome region (PWCR/ANCR, 15q11.2-12), meningioma chromosome region (MGCR, 22q12-13), and fragile X chromosome region (FRAXA, Xq27.3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP740604.RAGMKFBEhtvVtbWUxTOtG8gjBtiaN07EcfQBZESAo_TQY130_provenance.
- NP740604.RAGMKFBEhtvVtbWUxTOtG8gjBtiaN07EcfQBZESAo_TQY130_assertion evidence source_evidence_literature NP740604.RAGMKFBEhtvVtbWUxTOtG8gjBtiaN07EcfQBZESAo_TQY130_provenance.
- NP740604.RAGMKFBEhtvVtbWUxTOtG8gjBtiaN07EcfQBZESAo_TQY130_assertion SIO_000772 2159949 NP740604.RAGMKFBEhtvVtbWUxTOtG8gjBtiaN07EcfQBZESAo_TQY130_provenance.
- NP740604.RAGMKFBEhtvVtbWUxTOtG8gjBtiaN07EcfQBZESAo_TQY130_assertion wasDerivedFrom befree-20140225 NP740604.RAGMKFBEhtvVtbWUxTOtG8gjBtiaN07EcfQBZESAo_TQY130_provenance.
- NP740604.RAGMKFBEhtvVtbWUxTOtG8gjBtiaN07EcfQBZESAo_TQY130_assertion wasGeneratedBy ECO_0000203 NP740604.RAGMKFBEhtvVtbWUxTOtG8gjBtiaN07EcfQBZESAo_TQY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP740604.RAGMKFBEhtvVtbWUxTOtG8gjBtiaN07EcfQBZESAo_TQY130_provenance.