Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP436121.RA_0Kv-rtz5mEcF8BDzkvQoBGSUxC4rUnIYc_VLbN8OEM130_assertion> ?p ?o ?g. }
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- NP436121.RA_0Kv-rtz5mEcF8BDzkvQoBGSUxC4rUnIYc_VLbN8OEM130_assertion type Assertion NP436121.RA_0Kv-rtz5mEcF8BDzkvQoBGSUxC4rUnIYc_VLbN8OEM130_head.
- NP436121.RA_0Kv-rtz5mEcF8BDzkvQoBGSUxC4rUnIYc_VLbN8OEM130_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." NP436121.RA_0Kv-rtz5mEcF8BDzkvQoBGSUxC4rUnIYc_VLbN8OEM130_provenance.
- NP436121.RA_0Kv-rtz5mEcF8BDzkvQoBGSUxC4rUnIYc_VLbN8OEM130_assertion evidence source_evidence_literature NP436121.RA_0Kv-rtz5mEcF8BDzkvQoBGSUxC4rUnIYc_VLbN8OEM130_provenance.
- NP436121.RA_0Kv-rtz5mEcF8BDzkvQoBGSUxC4rUnIYc_VLbN8OEM130_assertion SIO_000772 20447141 NP436121.RA_0Kv-rtz5mEcF8BDzkvQoBGSUxC4rUnIYc_VLbN8OEM130_provenance.
- NP436121.RA_0Kv-rtz5mEcF8BDzkvQoBGSUxC4rUnIYc_VLbN8OEM130_assertion wasDerivedFrom befree-20140225 NP436121.RA_0Kv-rtz5mEcF8BDzkvQoBGSUxC4rUnIYc_VLbN8OEM130_provenance.
- NP436121.RA_0Kv-rtz5mEcF8BDzkvQoBGSUxC4rUnIYc_VLbN8OEM130_assertion wasGeneratedBy ECO_0000203 NP436121.RA_0Kv-rtz5mEcF8BDzkvQoBGSUxC4rUnIYc_VLbN8OEM130_provenance.