Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP636224.RAFzGAU07Qz6RflVtl8ut0T1mzwT3ly8XermzY_sRKOsc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP636224.RAFzGAU07Qz6RflVtl8ut0T1mzwT3ly8XermzY_sRKOsc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP636224.RAFzGAU07Qz6RflVtl8ut0T1mzwT3ly8XermzY_sRKOsc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP636224.RAFzGAU07Qz6RflVtl8ut0T1mzwT3ly8XermzY_sRKOsc130_provenance.
- NP636224.RAFzGAU07Qz6RflVtl8ut0T1mzwT3ly8XermzY_sRKOsc130_assertion description "[Recently, mutations in the CXCR4 chemokine receptor gene were identified in a dominantly inherited immunodeficiency disease, WHIM syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP636224.RAFzGAU07Qz6RflVtl8ut0T1mzwT3ly8XermzY_sRKOsc130_provenance.
- NP636224.RAFzGAU07Qz6RflVtl8ut0T1mzwT3ly8XermzY_sRKOsc130_assertion evidence source_evidence_literature NP636224.RAFzGAU07Qz6RflVtl8ut0T1mzwT3ly8XermzY_sRKOsc130_provenance.
- NP636224.RAFzGAU07Qz6RflVtl8ut0T1mzwT3ly8XermzY_sRKOsc130_assertion SIO_000772 15661033 NP636224.RAFzGAU07Qz6RflVtl8ut0T1mzwT3ly8XermzY_sRKOsc130_provenance.
- NP636224.RAFzGAU07Qz6RflVtl8ut0T1mzwT3ly8XermzY_sRKOsc130_assertion wasDerivedFrom befree-20140225 NP636224.RAFzGAU07Qz6RflVtl8ut0T1mzwT3ly8XermzY_sRKOsc130_provenance.
- NP636224.RAFzGAU07Qz6RflVtl8ut0T1mzwT3ly8XermzY_sRKOsc130_assertion wasGeneratedBy ECO_0000203 NP636224.RAFzGAU07Qz6RflVtl8ut0T1mzwT3ly8XermzY_sRKOsc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP636224.RAFzGAU07Qz6RflVtl8ut0T1mzwT3ly8XermzY_sRKOsc130_provenance.