Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP636224.RAFzGAU07Qz6RflVtl8ut0T1mzwT3ly8XermzY_sRKOsc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP636224.RAFzGAU07Qz6RflVtl8ut0T1mzwT3ly8XermzY_sRKOsc130_assertion type Assertion NP636224.RAFzGAU07Qz6RflVtl8ut0T1mzwT3ly8XermzY_sRKOsc130_head.
- 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.