Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP333517.RAF_aVHMOuQ4ILCfg63L-3a0yXJxwwK9BUDDOu1fSYkUE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP333517.RAF_aVHMOuQ4ILCfg63L-3a0yXJxwwK9BUDDOu1fSYkUE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP333517.RAF_aVHMOuQ4ILCfg63L-3a0yXJxwwK9BUDDOu1fSYkUE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP333517.RAF_aVHMOuQ4ILCfg63L-3a0yXJxwwK9BUDDOu1fSYkUE130_provenance.
- NP333517.RAF_aVHMOuQ4ILCfg63L-3a0yXJxwwK9BUDDOu1fSYkUE130_assertion description "[Genotyping data, the absence of a significant difference in allele frequencies between patients and controls, and survival analyses suggest an increased susceptibility for ARMD in CST3 B/B homozygotes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333517.RAF_aVHMOuQ4ILCfg63L-3a0yXJxwwK9BUDDOu1fSYkUE130_provenance.
- NP333517.RAF_aVHMOuQ4ILCfg63L-3a0yXJxwwK9BUDDOu1fSYkUE130_assertion evidence source_evidence_literature NP333517.RAF_aVHMOuQ4ILCfg63L-3a0yXJxwwK9BUDDOu1fSYkUE130_provenance.
- NP333517.RAF_aVHMOuQ4ILCfg63L-3a0yXJxwwK9BUDDOu1fSYkUE130_assertion SIO_000772 11815350 NP333517.RAF_aVHMOuQ4ILCfg63L-3a0yXJxwwK9BUDDOu1fSYkUE130_provenance.
- NP333517.RAF_aVHMOuQ4ILCfg63L-3a0yXJxwwK9BUDDOu1fSYkUE130_assertion wasDerivedFrom befree-20150227 NP333517.RAF_aVHMOuQ4ILCfg63L-3a0yXJxwwK9BUDDOu1fSYkUE130_provenance.
- NP333517.RAF_aVHMOuQ4ILCfg63L-3a0yXJxwwK9BUDDOu1fSYkUE130_assertion wasGeneratedBy ECO_0000203 NP333517.RAF_aVHMOuQ4ILCfg63L-3a0yXJxwwK9BUDDOu1fSYkUE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP333517.RAF_aVHMOuQ4ILCfg63L-3a0yXJxwwK9BUDDOu1fSYkUE130_provenance.