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- NP736048.RAhvWtGc497wvddFFp87PX10CL_KKGoSdmSMT4ibhLcfc130_assertion type Assertion NP736048.RAhvWtGc497wvddFFp87PX10CL_KKGoSdmSMT4ibhLcfc130_head.
- NP736048.RAhvWtGc497wvddFFp87PX10CL_KKGoSdmSMT4ibhLcfc130_assertion description "[Hypomorphic mutations in NBN (previously known as NBS1) and MRE11A give rise to the autosomal-recessive diseases Nijmegen breakage syndrome (NBS) and ataxia-telangiectasia-like disorder (ATLD), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP736048.RAhvWtGc497wvddFFp87PX10CL_KKGoSdmSMT4ibhLcfc130_provenance.
- NP736048.RAhvWtGc497wvddFFp87PX10CL_KKGoSdmSMT4ibhLcfc130_assertion evidence source_evidence_literature NP736048.RAhvWtGc497wvddFFp87PX10CL_KKGoSdmSMT4ibhLcfc130_provenance.
- NP736048.RAhvWtGc497wvddFFp87PX10CL_KKGoSdmSMT4ibhLcfc130_assertion SIO_000772 19409520 NP736048.RAhvWtGc497wvddFFp87PX10CL_KKGoSdmSMT4ibhLcfc130_provenance.
- NP736048.RAhvWtGc497wvddFFp87PX10CL_KKGoSdmSMT4ibhLcfc130_assertion wasDerivedFrom befree-2016 NP736048.RAhvWtGc497wvddFFp87PX10CL_KKGoSdmSMT4ibhLcfc130_provenance.
- NP736048.RAhvWtGc497wvddFFp87PX10CL_KKGoSdmSMT4ibhLcfc130_assertion wasGeneratedBy ECO_0000203 NP736048.RAhvWtGc497wvddFFp87PX10CL_KKGoSdmSMT4ibhLcfc130_provenance.