Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP799772.RAfD_CMNRCX88zp3nQP37jpcJrEUcdhqMk-1aNM3e-nxA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP799772.RAfD_CMNRCX88zp3nQP37jpcJrEUcdhqMk-1aNM3e-nxA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP799772.RAfD_CMNRCX88zp3nQP37jpcJrEUcdhqMk-1aNM3e-nxA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP799772.RAfD_CMNRCX88zp3nQP37jpcJrEUcdhqMk-1aNM3e-nxA130_provenance.
- NP799772.RAfD_CMNRCX88zp3nQP37jpcJrEUcdhqMk-1aNM3e-nxA130_assertion description "[We have examined a restriction fragment length polymorphism at the thyroglobulin locus in a patient with Langer-Giedion syndrome and 8q deletion in order to: (1) localize the Langer-Giedion deletion more precisely, (2) define the relative map positions of the thyroglobulin gene and the Langer-Giedion locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP799772.RAfD_CMNRCX88zp3nQP37jpcJrEUcdhqMk-1aNM3e-nxA130_provenance.
- NP799772.RAfD_CMNRCX88zp3nQP37jpcJrEUcdhqMk-1aNM3e-nxA130_assertion evidence source_evidence_literature NP799772.RAfD_CMNRCX88zp3nQP37jpcJrEUcdhqMk-1aNM3e-nxA130_provenance.
- NP799772.RAfD_CMNRCX88zp3nQP37jpcJrEUcdhqMk-1aNM3e-nxA130_assertion SIO_000772 2876948 NP799772.RAfD_CMNRCX88zp3nQP37jpcJrEUcdhqMk-1aNM3e-nxA130_provenance.
- NP799772.RAfD_CMNRCX88zp3nQP37jpcJrEUcdhqMk-1aNM3e-nxA130_assertion wasDerivedFrom befree-20140225 NP799772.RAfD_CMNRCX88zp3nQP37jpcJrEUcdhqMk-1aNM3e-nxA130_provenance.
- NP799772.RAfD_CMNRCX88zp3nQP37jpcJrEUcdhqMk-1aNM3e-nxA130_assertion wasGeneratedBy ECO_0000203 NP799772.RAfD_CMNRCX88zp3nQP37jpcJrEUcdhqMk-1aNM3e-nxA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP799772.RAfD_CMNRCX88zp3nQP37jpcJrEUcdhqMk-1aNM3e-nxA130_provenance.