Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP781208.RA9QoiYtqADZq8BARE33ODaLQjVqoFEsVyysG5nqnOteI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP781208.RA9QoiYtqADZq8BARE33ODaLQjVqoFEsVyysG5nqnOteI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP781208.RA9QoiYtqADZq8BARE33ODaLQjVqoFEsVyysG5nqnOteI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP781208.RA9QoiYtqADZq8BARE33ODaLQjVqoFEsVyysG5nqnOteI130_provenance.
- NP781208.RA9QoiYtqADZq8BARE33ODaLQjVqoFEsVyysG5nqnOteI130_assertion description "[St�ve-Wiedemann syndrome (SWS, OMIM 601559) is a severe autosomal recessive condition caused by mutations in the leukemia inhibitory receptor (LIFR) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781208.RA9QoiYtqADZq8BARE33ODaLQjVqoFEsVyysG5nqnOteI130_provenance.
- NP781208.RA9QoiYtqADZq8BARE33ODaLQjVqoFEsVyysG5nqnOteI130_assertion evidence source_evidence_literature NP781208.RA9QoiYtqADZq8BARE33ODaLQjVqoFEsVyysG5nqnOteI130_provenance.
- NP781208.RA9QoiYtqADZq8BARE33ODaLQjVqoFEsVyysG5nqnOteI130_assertion SIO_000772 20447141 NP781208.RA9QoiYtqADZq8BARE33ODaLQjVqoFEsVyysG5nqnOteI130_provenance.
- NP781208.RA9QoiYtqADZq8BARE33ODaLQjVqoFEsVyysG5nqnOteI130_assertion wasDerivedFrom befree-20140225 NP781208.RA9QoiYtqADZq8BARE33ODaLQjVqoFEsVyysG5nqnOteI130_provenance.
- NP781208.RA9QoiYtqADZq8BARE33ODaLQjVqoFEsVyysG5nqnOteI130_assertion wasGeneratedBy ECO_0000203 NP781208.RA9QoiYtqADZq8BARE33ODaLQjVqoFEsVyysG5nqnOteI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP781208.RA9QoiYtqADZq8BARE33ODaLQjVqoFEsVyysG5nqnOteI130_provenance.