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- NP443705.RAp_0kesmQU2KJEPq9cgsg1klPfUjF-9vOH8_Bzh3cycE130_assertion type Assertion NP443705.RAp_0kesmQU2KJEPq9cgsg1klPfUjF-9vOH8_Bzh3cycE130_head.
- NP443705.RAp_0kesmQU2KJEPq9cgsg1klPfUjF-9vOH8_Bzh3cycE130_assertion wasGeneratedBy ECO_0000203 NP443705.RAp_0kesmQU2KJEPq9cgsg1klPfUjF-9vOH8_Bzh3cycE130_provenance.
- NP443705.RAp_0kesmQU2KJEPq9cgsg1klPfUjF-9vOH8_Bzh3cycE130_assertion wasDerivedFrom befree-20150227 NP443705.RAp_0kesmQU2KJEPq9cgsg1klPfUjF-9vOH8_Bzh3cycE130_provenance.
- NP443705.RAp_0kesmQU2KJEPq9cgsg1klPfUjF-9vOH8_Bzh3cycE130_assertion SIO_000772 8034555 NP443705.RAp_0kesmQU2KJEPq9cgsg1klPfUjF-9vOH8_Bzh3cycE130_provenance.
- NP443705.RAp_0kesmQU2KJEPq9cgsg1klPfUjF-9vOH8_Bzh3cycE130_assertion evidence source_evidence_literature NP443705.RAp_0kesmQU2KJEPq9cgsg1klPfUjF-9vOH8_Bzh3cycE130_provenance.
- NP443705.RAp_0kesmQU2KJEPq9cgsg1klPfUjF-9vOH8_Bzh3cycE130_assertion description "[In the rare cases with severe beta-thalassemia mutations, the normal levels of HbA2 may be due to coinheritance of as yet undefined delta thalassemia mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP443705.RAp_0kesmQU2KJEPq9cgsg1klPfUjF-9vOH8_Bzh3cycE130_provenance.