Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP207.RARdWpib2ofoy5nbuD2Xv7g1Ovtt_vxYbtlLlwiJPzKEI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP207.RARdWpib2ofoy5nbuD2Xv7g1Ovtt_vxYbtlLlwiJPzKEI130_assertion type Assertion NP207.RARdWpib2ofoy5nbuD2Xv7g1Ovtt_vxYbtlLlwiJPzKEI130_head.
- NP207.RARdWpib2ofoy5nbuD2Xv7g1Ovtt_vxYbtlLlwiJPzKEI130_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." NP207.RARdWpib2ofoy5nbuD2Xv7g1Ovtt_vxYbtlLlwiJPzKEI130_provenance.
- NP207.RARdWpib2ofoy5nbuD2Xv7g1Ovtt_vxYbtlLlwiJPzKEI130_assertion evidence source_evidence_curated NP207.RARdWpib2ofoy5nbuD2Xv7g1Ovtt_vxYbtlLlwiJPzKEI130_provenance.
- NP207.RARdWpib2ofoy5nbuD2Xv7g1Ovtt_vxYbtlLlwiJPzKEI130_assertion SIO_000772 8227344 NP207.RARdWpib2ofoy5nbuD2Xv7g1Ovtt_vxYbtlLlwiJPzKEI130_provenance.
- NP207.RARdWpib2ofoy5nbuD2Xv7g1Ovtt_vxYbtlLlwiJPzKEI130_assertion wasDerivedFrom uniprot-20130724 NP207.RARdWpib2ofoy5nbuD2Xv7g1Ovtt_vxYbtlLlwiJPzKEI130_provenance.
- NP207.RARdWpib2ofoy5nbuD2Xv7g1Ovtt_vxYbtlLlwiJPzKEI130_assertion wasGeneratedBy ECO_0000218 NP207.RARdWpib2ofoy5nbuD2Xv7g1Ovtt_vxYbtlLlwiJPzKEI130_provenance.