Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP222774.RAMCw3ST3NFY1qd0Ghe39lDRlDsyzudleLJrNO5Io2OFs130_assertion> ?p ?o ?g. }
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- NP222774.RAMCw3ST3NFY1qd0Ghe39lDRlDsyzudleLJrNO5Io2OFs130_assertion type Assertion NP222774.RAMCw3ST3NFY1qd0Ghe39lDRlDsyzudleLJrNO5Io2OFs130_head.
- NP222774.RAMCw3ST3NFY1qd0Ghe39lDRlDsyzudleLJrNO5Io2OFs130_assertion description "[Novel splicing, missense, and deletion mutations in seven adenosine deaminase-deficient patients with late/delayed onset of combined immunodeficiency disease. Contribution of genotype to phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222774.RAMCw3ST3NFY1qd0Ghe39lDRlDsyzudleLJrNO5Io2OFs130_provenance.
- NP222774.RAMCw3ST3NFY1qd0Ghe39lDRlDsyzudleLJrNO5Io2OFs130_assertion evidence source_evidence_literature NP222774.RAMCw3ST3NFY1qd0Ghe39lDRlDsyzudleLJrNO5Io2OFs130_provenance.
- NP222774.RAMCw3ST3NFY1qd0Ghe39lDRlDsyzudleLJrNO5Io2OFs130_assertion SIO_000772 8227344 NP222774.RAMCw3ST3NFY1qd0Ghe39lDRlDsyzudleLJrNO5Io2OFs130_provenance.
- NP222774.RAMCw3ST3NFY1qd0Ghe39lDRlDsyzudleLJrNO5Io2OFs130_assertion wasDerivedFrom befree-20150227 NP222774.RAMCw3ST3NFY1qd0Ghe39lDRlDsyzudleLJrNO5Io2OFs130_provenance.
- NP222774.RAMCw3ST3NFY1qd0Ghe39lDRlDsyzudleLJrNO5Io2OFs130_assertion wasGeneratedBy ECO_0000203 NP222774.RAMCw3ST3NFY1qd0Ghe39lDRlDsyzudleLJrNO5Io2OFs130_provenance.