Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP514450.RAFRLSV7Z34QSRgafk18VjUmZ6IFTo_3LFcTafNHJl_mE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP514450.RAFRLSV7Z34QSRgafk18VjUmZ6IFTo_3LFcTafNHJl_mE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP514450.RAFRLSV7Z34QSRgafk18VjUmZ6IFTo_3LFcTafNHJl_mE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP514450.RAFRLSV7Z34QSRgafk18VjUmZ6IFTo_3LFcTafNHJl_mE130_provenance.
- NP514450.RAFRLSV7Z34QSRgafk18VjUmZ6IFTo_3LFcTafNHJl_mE130_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." NP514450.RAFRLSV7Z34QSRgafk18VjUmZ6IFTo_3LFcTafNHJl_mE130_provenance.
- NP514450.RAFRLSV7Z34QSRgafk18VjUmZ6IFTo_3LFcTafNHJl_mE130_assertion evidence source_evidence_literature NP514450.RAFRLSV7Z34QSRgafk18VjUmZ6IFTo_3LFcTafNHJl_mE130_provenance.
- NP514450.RAFRLSV7Z34QSRgafk18VjUmZ6IFTo_3LFcTafNHJl_mE130_assertion SIO_000772 16175500 NP514450.RAFRLSV7Z34QSRgafk18VjUmZ6IFTo_3LFcTafNHJl_mE130_provenance.
- NP514450.RAFRLSV7Z34QSRgafk18VjUmZ6IFTo_3LFcTafNHJl_mE130_assertion wasDerivedFrom befree-2016 NP514450.RAFRLSV7Z34QSRgafk18VjUmZ6IFTo_3LFcTafNHJl_mE130_provenance.
- NP514450.RAFRLSV7Z34QSRgafk18VjUmZ6IFTo_3LFcTafNHJl_mE130_assertion wasGeneratedBy ECO_0000203 NP514450.RAFRLSV7Z34QSRgafk18VjUmZ6IFTo_3LFcTafNHJl_mE130_provenance.
- befree-2016 importedOn "2016-02-19" NP514450.RAFRLSV7Z34QSRgafk18VjUmZ6IFTo_3LFcTafNHJl_mE130_provenance.