Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP808984.RALTs9v4gVx_lD-Xgnd7gzx6LMh1I02qTrGf-ZTMUEp3s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP808984.RALTs9v4gVx_lD-Xgnd7gzx6LMh1I02qTrGf-ZTMUEp3s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP808984.RALTs9v4gVx_lD-Xgnd7gzx6LMh1I02qTrGf-ZTMUEp3s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP808984.RALTs9v4gVx_lD-Xgnd7gzx6LMh1I02qTrGf-ZTMUEp3s130_provenance.
- NP808984.RALTs9v4gVx_lD-Xgnd7gzx6LMh1I02qTrGf-ZTMUEp3s130_assertion description "[We identified 12 patients with LWD who presented with a novel class of PAR1 deletions that did not include SHOX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP808984.RALTs9v4gVx_lD-Xgnd7gzx6LMh1I02qTrGf-ZTMUEp3s130_provenance.
- NP808984.RALTs9v4gVx_lD-Xgnd7gzx6LMh1I02qTrGf-ZTMUEp3s130_assertion evidence source_evidence_literature NP808984.RALTs9v4gVx_lD-Xgnd7gzx6LMh1I02qTrGf-ZTMUEp3s130_provenance.
- NP808984.RALTs9v4gVx_lD-Xgnd7gzx6LMh1I02qTrGf-ZTMUEp3s130_assertion SIO_000772 16175500 NP808984.RALTs9v4gVx_lD-Xgnd7gzx6LMh1I02qTrGf-ZTMUEp3s130_provenance.
- NP808984.RALTs9v4gVx_lD-Xgnd7gzx6LMh1I02qTrGf-ZTMUEp3s130_assertion wasDerivedFrom befree-20150227 NP808984.RALTs9v4gVx_lD-Xgnd7gzx6LMh1I02qTrGf-ZTMUEp3s130_provenance.
- NP808984.RALTs9v4gVx_lD-Xgnd7gzx6LMh1I02qTrGf-ZTMUEp3s130_assertion wasGeneratedBy ECO_0000203 NP808984.RALTs9v4gVx_lD-Xgnd7gzx6LMh1I02qTrGf-ZTMUEp3s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP808984.RALTs9v4gVx_lD-Xgnd7gzx6LMh1I02qTrGf-ZTMUEp3s130_provenance.