Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP536556.RAbUnFY0iXrCWJh88jJs52HvWE-Y3a_xYeOAZO23VCXXE130_assertion> ?p ?o ?g. }
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- NP536556.RAbUnFY0iXrCWJh88jJs52HvWE-Y3a_xYeOAZO23VCXXE130_assertion type Assertion NP536556.RAbUnFY0iXrCWJh88jJs52HvWE-Y3a_xYeOAZO23VCXXE130_head.
- NP536556.RAbUnFY0iXrCWJh88jJs52HvWE-Y3a_xYeOAZO23VCXXE130_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." NP536556.RAbUnFY0iXrCWJh88jJs52HvWE-Y3a_xYeOAZO23VCXXE130_provenance.
- NP536556.RAbUnFY0iXrCWJh88jJs52HvWE-Y3a_xYeOAZO23VCXXE130_assertion evidence source_evidence_literature NP536556.RAbUnFY0iXrCWJh88jJs52HvWE-Y3a_xYeOAZO23VCXXE130_provenance.
- NP536556.RAbUnFY0iXrCWJh88jJs52HvWE-Y3a_xYeOAZO23VCXXE130_assertion SIO_000772 20447141 NP536556.RAbUnFY0iXrCWJh88jJs52HvWE-Y3a_xYeOAZO23VCXXE130_provenance.
- NP536556.RAbUnFY0iXrCWJh88jJs52HvWE-Y3a_xYeOAZO23VCXXE130_assertion wasDerivedFrom befree-20150227 NP536556.RAbUnFY0iXrCWJh88jJs52HvWE-Y3a_xYeOAZO23VCXXE130_provenance.
- NP536556.RAbUnFY0iXrCWJh88jJs52HvWE-Y3a_xYeOAZO23VCXXE130_assertion wasGeneratedBy ECO_0000203 NP536556.RAbUnFY0iXrCWJh88jJs52HvWE-Y3a_xYeOAZO23VCXXE130_provenance.