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- NP206389.RAWulyuMDfeUdBW9ruymmoHIcGeezW0fDHUlP5K6X3qZo130_assertion type Assertion NP206389.RAWulyuMDfeUdBW9ruymmoHIcGeezW0fDHUlP5K6X3qZo130_head.
- NP206389.RAWulyuMDfeUdBW9ruymmoHIcGeezW0fDHUlP5K6X3qZo130_assertion wasGeneratedBy ECO_0000203 NP206389.RAWulyuMDfeUdBW9ruymmoHIcGeezW0fDHUlP5K6X3qZo130_provenance.
- NP206389.RAWulyuMDfeUdBW9ruymmoHIcGeezW0fDHUlP5K6X3qZo130_assertion wasDerivedFrom befree-20140225 NP206389.RAWulyuMDfeUdBW9ruymmoHIcGeezW0fDHUlP5K6X3qZo130_provenance.
- NP206389.RAWulyuMDfeUdBW9ruymmoHIcGeezW0fDHUlP5K6X3qZo130_assertion SIO_000772 11257260 NP206389.RAWulyuMDfeUdBW9ruymmoHIcGeezW0fDHUlP5K6X3qZo130_provenance.
- NP206389.RAWulyuMDfeUdBW9ruymmoHIcGeezW0fDHUlP5K6X3qZo130_assertion evidence source_evidence_literature NP206389.RAWulyuMDfeUdBW9ruymmoHIcGeezW0fDHUlP5K6X3qZo130_provenance.
- NP206389.RAWulyuMDfeUdBW9ruymmoHIcGeezW0fDHUlP5K6X3qZo130_assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP206389.RAWulyuMDfeUdBW9ruymmoHIcGeezW0fDHUlP5K6X3qZo130_provenance.