Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP977632.RAB-FpbEZtSZjF2AyXxAteNXUync16zEE3LP-vBvt-_8Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP977632.RAB-FpbEZtSZjF2AyXxAteNXUync16zEE3LP-vBvt-_8Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP977632.RAB-FpbEZtSZjF2AyXxAteNXUync16zEE3LP-vBvt-_8Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP977632.RAB-FpbEZtSZjF2AyXxAteNXUync16zEE3LP-vBvt-_8Q130_provenance.
- NP977632.RAB-FpbEZtSZjF2AyXxAteNXUync16zEE3LP-vBvt-_8Q130_assertion description "[We focus on a newly described human immunodeficiency disorder called radiosensitivity, immunodeficiency dysmorphic features and learning difficulties (RIDDLE) syndrome, with particular reference to the function of the defective gene, RNF168.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977632.RAB-FpbEZtSZjF2AyXxAteNXUync16zEE3LP-vBvt-_8Q130_provenance.
- NP977632.RAB-FpbEZtSZjF2AyXxAteNXUync16zEE3LP-vBvt-_8Q130_assertion evidence source_evidence_literature NP977632.RAB-FpbEZtSZjF2AyXxAteNXUync16zEE3LP-vBvt-_8Q130_provenance.
- NP977632.RAB-FpbEZtSZjF2AyXxAteNXUync16zEE3LP-vBvt-_8Q130_assertion SIO_000772 21426255 NP977632.RAB-FpbEZtSZjF2AyXxAteNXUync16zEE3LP-vBvt-_8Q130_provenance.
- NP977632.RAB-FpbEZtSZjF2AyXxAteNXUync16zEE3LP-vBvt-_8Q130_assertion wasDerivedFrom befree-20150227 NP977632.RAB-FpbEZtSZjF2AyXxAteNXUync16zEE3LP-vBvt-_8Q130_provenance.
- NP977632.RAB-FpbEZtSZjF2AyXxAteNXUync16zEE3LP-vBvt-_8Q130_assertion wasGeneratedBy ECO_0000203 NP977632.RAB-FpbEZtSZjF2AyXxAteNXUync16zEE3LP-vBvt-_8Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP977632.RAB-FpbEZtSZjF2AyXxAteNXUync16zEE3LP-vBvt-_8Q130_provenance.