Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP100197.RAeztRMeVtwsyOSWeerV4uH2lvKYWdvwbD1i1FUvurgmo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP100197.RAeztRMeVtwsyOSWeerV4uH2lvKYWdvwbD1i1FUvurgmo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP100197.RAeztRMeVtwsyOSWeerV4uH2lvKYWdvwbD1i1FUvurgmo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP100197.RAeztRMeVtwsyOSWeerV4uH2lvKYWdvwbD1i1FUvurgmo130_provenance.
- NP100197.RAeztRMeVtwsyOSWeerV4uH2lvKYWdvwbD1i1FUvurgmo130_assertion description "[Our studies suggest that the frequency of the c2 alleles in Polish population is low.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP100197.RAeztRMeVtwsyOSWeerV4uH2lvKYWdvwbD1i1FUvurgmo130_provenance.
- NP100197.RAeztRMeVtwsyOSWeerV4uH2lvKYWdvwbD1i1FUvurgmo130_assertion evidence source_evidence_literature NP100197.RAeztRMeVtwsyOSWeerV4uH2lvKYWdvwbD1i1FUvurgmo130_provenance.
- NP100197.RAeztRMeVtwsyOSWeerV4uH2lvKYWdvwbD1i1FUvurgmo130_assertion SIO_000772 16634857 NP100197.RAeztRMeVtwsyOSWeerV4uH2lvKYWdvwbD1i1FUvurgmo130_provenance.
- NP100197.RAeztRMeVtwsyOSWeerV4uH2lvKYWdvwbD1i1FUvurgmo130_assertion wasDerivedFrom gad-20150221 NP100197.RAeztRMeVtwsyOSWeerV4uH2lvKYWdvwbD1i1FUvurgmo130_provenance.
- NP100197.RAeztRMeVtwsyOSWeerV4uH2lvKYWdvwbD1i1FUvurgmo130_assertion wasGeneratedBy ECO_0000203 NP100197.RAeztRMeVtwsyOSWeerV4uH2lvKYWdvwbD1i1FUvurgmo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP100197.RAeztRMeVtwsyOSWeerV4uH2lvKYWdvwbD1i1FUvurgmo130_provenance.