Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1045488.RAvkP9h3xgkVhF2YYOGm6GMTc3ZCk63t-YjqCBTRYGCco130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1045488.RAvkP9h3xgkVhF2YYOGm6GMTc3ZCk63t-YjqCBTRYGCco130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1045488.RAvkP9h3xgkVhF2YYOGm6GMTc3ZCk63t-YjqCBTRYGCco130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1045488.RAvkP9h3xgkVhF2YYOGm6GMTc3ZCk63t-YjqCBTRYGCco130_provenance.
- befree-2016 importedOn "2016-02-19" NP1045488.RAvkP9h3xgkVhF2YYOGm6GMTc3ZCk63t-YjqCBTRYGCco130_provenance.
- NP1045488.RAvkP9h3xgkVhF2YYOGm6GMTc3ZCk63t-YjqCBTRYGCco130_assertion wasGeneratedBy ECO_0000203 NP1045488.RAvkP9h3xgkVhF2YYOGm6GMTc3ZCk63t-YjqCBTRYGCco130_provenance.
- NP1045488.RAvkP9h3xgkVhF2YYOGm6GMTc3ZCk63t-YjqCBTRYGCco130_assertion wasDerivedFrom befree-2016 NP1045488.RAvkP9h3xgkVhF2YYOGm6GMTc3ZCk63t-YjqCBTRYGCco130_provenance.
- NP1045488.RAvkP9h3xgkVhF2YYOGm6GMTc3ZCk63t-YjqCBTRYGCco130_assertion SIO_000772 23335808 NP1045488.RAvkP9h3xgkVhF2YYOGm6GMTc3ZCk63t-YjqCBTRYGCco130_provenance.
- NP1045488.RAvkP9h3xgkVhF2YYOGm6GMTc3ZCk63t-YjqCBTRYGCco130_assertion evidence source_evidence_literature NP1045488.RAvkP9h3xgkVhF2YYOGm6GMTc3ZCk63t-YjqCBTRYGCco130_provenance.
- NP1045488.RAvkP9h3xgkVhF2YYOGm6GMTc3ZCk63t-YjqCBTRYGCco130_assertion description "[14 of the deletions associated with ASD/ID overlap the coding regions of FBXO31 and MAP1LC3B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1045488.RAvkP9h3xgkVhF2YYOGm6GMTc3ZCk63t-YjqCBTRYGCco130_provenance.