Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP281155.RAnfNS1dRjrhslF_UCRT70cjJsE7Jbbcl_23vgzcsGdao130_assertion> ?p ?o ?g. }
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- NP281155.RAnfNS1dRjrhslF_UCRT70cjJsE7Jbbcl_23vgzcsGdao130_assertion type Assertion NP281155.RAnfNS1dRjrhslF_UCRT70cjJsE7Jbbcl_23vgzcsGdao130_head.
- NP281155.RAnfNS1dRjrhslF_UCRT70cjJsE7Jbbcl_23vgzcsGdao130_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." NP281155.RAnfNS1dRjrhslF_UCRT70cjJsE7Jbbcl_23vgzcsGdao130_provenance.
- NP281155.RAnfNS1dRjrhslF_UCRT70cjJsE7Jbbcl_23vgzcsGdao130_assertion evidence source_evidence_literature NP281155.RAnfNS1dRjrhslF_UCRT70cjJsE7Jbbcl_23vgzcsGdao130_provenance.
- NP281155.RAnfNS1dRjrhslF_UCRT70cjJsE7Jbbcl_23vgzcsGdao130_assertion SIO_000772 20447141 NP281155.RAnfNS1dRjrhslF_UCRT70cjJsE7Jbbcl_23vgzcsGdao130_provenance.
- NP281155.RAnfNS1dRjrhslF_UCRT70cjJsE7Jbbcl_23vgzcsGdao130_assertion wasDerivedFrom befree-20140225 NP281155.RAnfNS1dRjrhslF_UCRT70cjJsE7Jbbcl_23vgzcsGdao130_provenance.
- NP281155.RAnfNS1dRjrhslF_UCRT70cjJsE7Jbbcl_23vgzcsGdao130_assertion wasGeneratedBy ECO_0000203 NP281155.RAnfNS1dRjrhslF_UCRT70cjJsE7Jbbcl_23vgzcsGdao130_provenance.