Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP694491.RA68HyA7UEqB2eICklq5Zj-OmYkbIPBfvZ7UKTHhd3Ho0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP694491.RA68HyA7UEqB2eICklq5Zj-OmYkbIPBfvZ7UKTHhd3Ho0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP694491.RA68HyA7UEqB2eICklq5Zj-OmYkbIPBfvZ7UKTHhd3Ho0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP694491.RA68HyA7UEqB2eICklq5Zj-OmYkbIPBfvZ7UKTHhd3Ho0130_provenance.
- NP694491.RA68HyA7UEqB2eICklq5Zj-OmYkbIPBfvZ7UKTHhd3Ho0130_assertion description "[Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694491.RA68HyA7UEqB2eICklq5Zj-OmYkbIPBfvZ7UKTHhd3Ho0130_provenance.
- NP694491.RA68HyA7UEqB2eICklq5Zj-OmYkbIPBfvZ7UKTHhd3Ho0130_assertion evidence source_evidence_literature NP694491.RA68HyA7UEqB2eICklq5Zj-OmYkbIPBfvZ7UKTHhd3Ho0130_provenance.
- NP694491.RA68HyA7UEqB2eICklq5Zj-OmYkbIPBfvZ7UKTHhd3Ho0130_assertion SIO_000772 23778136 NP694491.RA68HyA7UEqB2eICklq5Zj-OmYkbIPBfvZ7UKTHhd3Ho0130_provenance.
- NP694491.RA68HyA7UEqB2eICklq5Zj-OmYkbIPBfvZ7UKTHhd3Ho0130_assertion wasDerivedFrom befree-20150227 NP694491.RA68HyA7UEqB2eICklq5Zj-OmYkbIPBfvZ7UKTHhd3Ho0130_provenance.
- NP694491.RA68HyA7UEqB2eICklq5Zj-OmYkbIPBfvZ7UKTHhd3Ho0130_assertion wasGeneratedBy ECO_0000203 NP694491.RA68HyA7UEqB2eICklq5Zj-OmYkbIPBfvZ7UKTHhd3Ho0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP694491.RA68HyA7UEqB2eICklq5Zj-OmYkbIPBfvZ7UKTHhd3Ho0130_provenance.