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- NP1295770.RAN5x66US-dpKDOIipQkaLnLPoMyV2QbeObOLHWlQ5AiE130_assertion type Assertion NP1295770.RAN5x66US-dpKDOIipQkaLnLPoMyV2QbeObOLHWlQ5AiE130_head.
- NP1295770.RAN5x66US-dpKDOIipQkaLnLPoMyV2QbeObOLHWlQ5AiE130_assertion description "[Association between the SMN2 gene copy number and clinical characteristics of patients with spinal muscular atrophy with homozygous deletion of exon 7 of the SMN1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295770.RAN5x66US-dpKDOIipQkaLnLPoMyV2QbeObOLHWlQ5AiE130_provenance.
- NP1295770.RAN5x66US-dpKDOIipQkaLnLPoMyV2QbeObOLHWlQ5AiE130_assertion evidence source_evidence_literature NP1295770.RAN5x66US-dpKDOIipQkaLnLPoMyV2QbeObOLHWlQ5AiE130_provenance.
- NP1295770.RAN5x66US-dpKDOIipQkaLnLPoMyV2QbeObOLHWlQ5AiE130_assertion SIO_000772 26665550 NP1295770.RAN5x66US-dpKDOIipQkaLnLPoMyV2QbeObOLHWlQ5AiE130_provenance.
- NP1295770.RAN5x66US-dpKDOIipQkaLnLPoMyV2QbeObOLHWlQ5AiE130_assertion wasDerivedFrom befree-2016 NP1295770.RAN5x66US-dpKDOIipQkaLnLPoMyV2QbeObOLHWlQ5AiE130_provenance.
- NP1295770.RAN5x66US-dpKDOIipQkaLnLPoMyV2QbeObOLHWlQ5AiE130_assertion wasGeneratedBy ECO_0000203 NP1295770.RAN5x66US-dpKDOIipQkaLnLPoMyV2QbeObOLHWlQ5AiE130_provenance.