Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP338434.RAqB50G2pswe0aC0K549FJvqTtnzx1YKJXPljvX0Xhp5Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP338434.RAqB50G2pswe0aC0K549FJvqTtnzx1YKJXPljvX0Xhp5Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP338434.RAqB50G2pswe0aC0K549FJvqTtnzx1YKJXPljvX0Xhp5Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP338434.RAqB50G2pswe0aC0K549FJvqTtnzx1YKJXPljvX0Xhp5Q130_provenance.
- NP338434.RAqB50G2pswe0aC0K549FJvqTtnzx1YKJXPljvX0Xhp5Q130_assertion description "[The rare CX3CR1 alleles were associated with an increased risk of BI and with reduced frequency of cardiovascular history.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP338434.RAqB50G2pswe0aC0K549FJvqTtnzx1YKJXPljvX0Xhp5Q130_provenance.
- NP338434.RAqB50G2pswe0aC0K549FJvqTtnzx1YKJXPljvX0Xhp5Q130_assertion evidence source_evidence_literature NP338434.RAqB50G2pswe0aC0K549FJvqTtnzx1YKJXPljvX0Xhp5Q130_provenance.
- NP338434.RAqB50G2pswe0aC0K549FJvqTtnzx1YKJXPljvX0Xhp5Q130_assertion SIO_000772 15681302 NP338434.RAqB50G2pswe0aC0K549FJvqTtnzx1YKJXPljvX0Xhp5Q130_provenance.
- NP338434.RAqB50G2pswe0aC0K549FJvqTtnzx1YKJXPljvX0Xhp5Q130_assertion wasDerivedFrom befree-20150227 NP338434.RAqB50G2pswe0aC0K549FJvqTtnzx1YKJXPljvX0Xhp5Q130_provenance.
- NP338434.RAqB50G2pswe0aC0K549FJvqTtnzx1YKJXPljvX0Xhp5Q130_assertion wasGeneratedBy ECO_0000203 NP338434.RAqB50G2pswe0aC0K549FJvqTtnzx1YKJXPljvX0Xhp5Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP338434.RAqB50G2pswe0aC0K549FJvqTtnzx1YKJXPljvX0Xhp5Q130_provenance.