Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP95162.RASZofVNz1hIUePbHvTy8inPbMgxB1wMID9NN0d0EoG5E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP95162.RASZofVNz1hIUePbHvTy8inPbMgxB1wMID9NN0d0EoG5E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP95162.RASZofVNz1hIUePbHvTy8inPbMgxB1wMID9NN0d0EoG5E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP95162.RASZofVNz1hIUePbHvTy8inPbMgxB1wMID9NN0d0EoG5E130_provenance.
- NP95162.RASZofVNz1hIUePbHvTy8inPbMgxB1wMID9NN0d0EoG5E130_assertion wasGeneratedBy ECO_0000203 NP95162.RASZofVNz1hIUePbHvTy8inPbMgxB1wMID9NN0d0EoG5E130_provenance.
- NP95162.RASZofVNz1hIUePbHvTy8inPbMgxB1wMID9NN0d0EoG5E130_assertion wasDerivedFrom gad-20130706 NP95162.RASZofVNz1hIUePbHvTy8inPbMgxB1wMID9NN0d0EoG5E130_provenance.
- NP95162.RASZofVNz1hIUePbHvTy8inPbMgxB1wMID9NN0d0EoG5E130_assertion SIO_000772 20436471 NP95162.RASZofVNz1hIUePbHvTy8inPbMgxB1wMID9NN0d0EoG5E130_provenance.
- NP95162.RASZofVNz1hIUePbHvTy8inPbMgxB1wMID9NN0d0EoG5E130_assertion evidence source_evidence_literature NP95162.RASZofVNz1hIUePbHvTy8inPbMgxB1wMID9NN0d0EoG5E130_provenance.
- NP95162.RASZofVNz1hIUePbHvTy8inPbMgxB1wMID9NN0d0EoG5E130_assertion description "[Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95162.RASZofVNz1hIUePbHvTy8inPbMgxB1wMID9NN0d0EoG5E130_provenance.
- gad-20130706 importedOn "2013-07-06" NP95162.RASZofVNz1hIUePbHvTy8inPbMgxB1wMID9NN0d0EoG5E130_provenance.