Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP810403.RAd88zJEAPGO2i3eGRHvqkZFU6N6yl8_K16DkplTsJChs130_assertion> ?p ?o ?g. }
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- NP810403.RAd88zJEAPGO2i3eGRHvqkZFU6N6yl8_K16DkplTsJChs130_assertion type Assertion NP810403.RAd88zJEAPGO2i3eGRHvqkZFU6N6yl8_K16DkplTsJChs130_head.
- NP810403.RAd88zJEAPGO2i3eGRHvqkZFU6N6yl8_K16DkplTsJChs130_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." NP810403.RAd88zJEAPGO2i3eGRHvqkZFU6N6yl8_K16DkplTsJChs130_provenance.
- NP810403.RAd88zJEAPGO2i3eGRHvqkZFU6N6yl8_K16DkplTsJChs130_assertion evidence source_evidence_literature NP810403.RAd88zJEAPGO2i3eGRHvqkZFU6N6yl8_K16DkplTsJChs130_provenance.
- NP810403.RAd88zJEAPGO2i3eGRHvqkZFU6N6yl8_K16DkplTsJChs130_assertion SIO_000772 20447141 NP810403.RAd88zJEAPGO2i3eGRHvqkZFU6N6yl8_K16DkplTsJChs130_provenance.
- NP810403.RAd88zJEAPGO2i3eGRHvqkZFU6N6yl8_K16DkplTsJChs130_assertion wasDerivedFrom befree-2016 NP810403.RAd88zJEAPGO2i3eGRHvqkZFU6N6yl8_K16DkplTsJChs130_provenance.
- NP810403.RAd88zJEAPGO2i3eGRHvqkZFU6N6yl8_K16DkplTsJChs130_assertion wasGeneratedBy ECO_0000203 NP810403.RAd88zJEAPGO2i3eGRHvqkZFU6N6yl8_K16DkplTsJChs130_provenance.