Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1007064.RAf6oCPQHLcI_oPGUJSpGhhW1n9-wom1PAXPK6EV-peuo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1007064.RAf6oCPQHLcI_oPGUJSpGhhW1n9-wom1PAXPK6EV-peuo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1007064.RAf6oCPQHLcI_oPGUJSpGhhW1n9-wom1PAXPK6EV-peuo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1007064.RAf6oCPQHLcI_oPGUJSpGhhW1n9-wom1PAXPK6EV-peuo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1007064.RAf6oCPQHLcI_oPGUJSpGhhW1n9-wom1PAXPK6EV-peuo130_provenance.
- NP1007064.RAf6oCPQHLcI_oPGUJSpGhhW1n9-wom1PAXPK6EV-peuo130_assertion wasGeneratedBy ECO_0000203 NP1007064.RAf6oCPQHLcI_oPGUJSpGhhW1n9-wom1PAXPK6EV-peuo130_provenance.
- NP1007064.RAf6oCPQHLcI_oPGUJSpGhhW1n9-wom1PAXPK6EV-peuo130_assertion wasDerivedFrom befree-20150227 NP1007064.RAf6oCPQHLcI_oPGUJSpGhhW1n9-wom1PAXPK6EV-peuo130_provenance.
- NP1007064.RAf6oCPQHLcI_oPGUJSpGhhW1n9-wom1PAXPK6EV-peuo130_assertion SIO_000772 15008838 NP1007064.RAf6oCPQHLcI_oPGUJSpGhhW1n9-wom1PAXPK6EV-peuo130_provenance.
- NP1007064.RAf6oCPQHLcI_oPGUJSpGhhW1n9-wom1PAXPK6EV-peuo130_assertion evidence source_evidence_literature NP1007064.RAf6oCPQHLcI_oPGUJSpGhhW1n9-wom1PAXPK6EV-peuo130_provenance.
- NP1007064.RAf6oCPQHLcI_oPGUJSpGhhW1n9-wom1PAXPK6EV-peuo130_assertion description "[We genotyped the INS-IGF2 VNTR [using the surrogate INS-23 HphI single nucleotide polymorphism (SNP)] in 823 Graves' disease (GD)/multiple sclerosis (MS) families, 1433 GD/MS patients and 837 healthy control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1007064.RAf6oCPQHLcI_oPGUJSpGhhW1n9-wom1PAXPK6EV-peuo130_provenance.