Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP939200.RA5VI8J0_m3LrjtM0avPaKnV6zllfi_Lz37KPVQd0arXw130_assertion> ?p ?o ?g. }
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- NP939200.RA5VI8J0_m3LrjtM0avPaKnV6zllfi_Lz37KPVQd0arXw130_assertion type Assertion NP939200.RA5VI8J0_m3LrjtM0avPaKnV6zllfi_Lz37KPVQd0arXw130_head.
- NP939200.RA5VI8J0_m3LrjtM0avPaKnV6zllfi_Lz37KPVQd0arXw130_assertion description "[Mutations in the Artemis gene are causative in a subset of human severe combined immunodeficiencies (SCIDs) and Artemis-deficient cells exhibit radiation sensitivity and defective V(D)J recombination, implicating Artemis function in non-homologous end joining (NHEJ).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939200.RA5VI8J0_m3LrjtM0avPaKnV6zllfi_Lz37KPVQd0arXw130_provenance.
- NP939200.RA5VI8J0_m3LrjtM0avPaKnV6zllfi_Lz37KPVQd0arXw130_assertion evidence source_evidence_literature NP939200.RA5VI8J0_m3LrjtM0avPaKnV6zllfi_Lz37KPVQd0arXw130_provenance.
- NP939200.RA5VI8J0_m3LrjtM0avPaKnV6zllfi_Lz37KPVQd0arXw130_assertion SIO_000772 15811628 NP939200.RA5VI8J0_m3LrjtM0avPaKnV6zllfi_Lz37KPVQd0arXw130_provenance.
- NP939200.RA5VI8J0_m3LrjtM0avPaKnV6zllfi_Lz37KPVQd0arXw130_assertion wasDerivedFrom befree-20150227 NP939200.RA5VI8J0_m3LrjtM0avPaKnV6zllfi_Lz37KPVQd0arXw130_provenance.
- NP939200.RA5VI8J0_m3LrjtM0avPaKnV6zllfi_Lz37KPVQd0arXw130_assertion wasGeneratedBy ECO_0000203 NP939200.RA5VI8J0_m3LrjtM0avPaKnV6zllfi_Lz37KPVQd0arXw130_provenance.