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- NP1216641.RAPbT3HP2SN-HP68XCFZ_Da_51BzGtC20OGc_kxPEFvOM130_assertion type Assertion NP1216641.RAPbT3HP2SN-HP68XCFZ_Da_51BzGtC20OGc_kxPEFvOM130_head.
- NP1216641.RAPbT3HP2SN-HP68XCFZ_Da_51BzGtC20OGc_kxPEFvOM130_assertion description "[Wiskott-Aldrich syndrome (WAS) is caused by mutations in the WAS gene and is characterized by immunodeficiency, eczema and microthrombocytopenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1216641.RAPbT3HP2SN-HP68XCFZ_Da_51BzGtC20OGc_kxPEFvOM130_provenance.
- NP1216641.RAPbT3HP2SN-HP68XCFZ_Da_51BzGtC20OGc_kxPEFvOM130_assertion evidence source_evidence_literature NP1216641.RAPbT3HP2SN-HP68XCFZ_Da_51BzGtC20OGc_kxPEFvOM130_provenance.
- NP1216641.RAPbT3HP2SN-HP68XCFZ_Da_51BzGtC20OGc_kxPEFvOM130_assertion SIO_000772 25187265 NP1216641.RAPbT3HP2SN-HP68XCFZ_Da_51BzGtC20OGc_kxPEFvOM130_provenance.
- NP1216641.RAPbT3HP2SN-HP68XCFZ_Da_51BzGtC20OGc_kxPEFvOM130_assertion wasDerivedFrom befree-2016 NP1216641.RAPbT3HP2SN-HP68XCFZ_Da_51BzGtC20OGc_kxPEFvOM130_provenance.
- NP1216641.RAPbT3HP2SN-HP68XCFZ_Da_51BzGtC20OGc_kxPEFvOM130_assertion wasGeneratedBy ECO_0000203 NP1216641.RAPbT3HP2SN-HP68XCFZ_Da_51BzGtC20OGc_kxPEFvOM130_provenance.