Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP475510.RACrb52fHgoTtXtxTMu_gfwtDdHBhr8UrSz_4MMk_FWsQ130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP475510.RACrb52fHgoTtXtxTMu_gfwtDdHBhr8UrSz_4MMk_FWsQ130_assertion type Assertion NP475510.RACrb52fHgoTtXtxTMu_gfwtDdHBhr8UrSz_4MMk_FWsQ130_head.
- NP475510.RACrb52fHgoTtXtxTMu_gfwtDdHBhr8UrSz_4MMk_FWsQ130_assertion description "[Direct duplication of 8p21.3-->p23.1: a cytogenetic anomaly associated with developmental delay without consistent clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475510.RACrb52fHgoTtXtxTMu_gfwtDdHBhr8UrSz_4MMk_FWsQ130_provenance.
- NP475510.RACrb52fHgoTtXtxTMu_gfwtDdHBhr8UrSz_4MMk_FWsQ130_assertion evidence source_evidence_literature NP475510.RACrb52fHgoTtXtxTMu_gfwtDdHBhr8UrSz_4MMk_FWsQ130_provenance.
- NP475510.RACrb52fHgoTtXtxTMu_gfwtDdHBhr8UrSz_4MMk_FWsQ130_assertion SIO_000772 11745996 NP475510.RACrb52fHgoTtXtxTMu_gfwtDdHBhr8UrSz_4MMk_FWsQ130_provenance.
- NP475510.RACrb52fHgoTtXtxTMu_gfwtDdHBhr8UrSz_4MMk_FWsQ130_assertion wasDerivedFrom befree-20140225 NP475510.RACrb52fHgoTtXtxTMu_gfwtDdHBhr8UrSz_4MMk_FWsQ130_provenance.
- NP475510.RACrb52fHgoTtXtxTMu_gfwtDdHBhr8UrSz_4MMk_FWsQ130_assertion wasGeneratedBy ECO_0000203 NP475510.RACrb52fHgoTtXtxTMu_gfwtDdHBhr8UrSz_4MMk_FWsQ130_provenance.