Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP475510.RACrb52fHgoTtXtxTMu_gfwtDdHBhr8UrSz_4MMk_FWsQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP475510.RACrb52fHgoTtXtxTMu_gfwtDdHBhr8UrSz_4MMk_FWsQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP475510.RACrb52fHgoTtXtxTMu_gfwtDdHBhr8UrSz_4MMk_FWsQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP475510.RACrb52fHgoTtXtxTMu_gfwtDdHBhr8UrSz_4MMk_FWsQ130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP475510.RACrb52fHgoTtXtxTMu_gfwtDdHBhr8UrSz_4MMk_FWsQ130_provenance.