Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_assertion> ?p ?o ?g. }
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- NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_assertion type Assertion NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_head.
- NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_assertion wasGeneratedBy ECO_0000203 NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_provenance.
- NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_assertion wasDerivedFrom befree-2016 NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_provenance.
- NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_assertion SIO_000772 1481806 NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_provenance.
- NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_assertion evidence source_evidence_literature NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_provenance.
- NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_assertion description "[A male patient with a de novo proximal interstitial deletion of the short arm of chromosome 1 (46XY, del(1)(p13p22.3) is described with multiple anomalies and developmental delay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP431035.RACNDfYbRpueg6W4wSEwsNEnF0DIzIM7DojQUZ5pK0gng130_provenance.