Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP526925.RA6ON5nQ96RNQe7LU_n5ZtC9YH-j1L7sb62lQaH0z_Wzw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP526925.RA6ON5nQ96RNQe7LU_n5ZtC9YH-j1L7sb62lQaH0z_Wzw130_assertion type Assertion NP526925.RA6ON5nQ96RNQe7LU_n5ZtC9YH-j1L7sb62lQaH0z_Wzw130_head.
- NP526925.RA6ON5nQ96RNQe7LU_n5ZtC9YH-j1L7sb62lQaH0z_Wzw130_assertion description "[Mutations in the haemoglobin beta-globin (HbB) and glucose-6-phosphate dehydrogenase (G6PD) genes cause widespread human genetic disorders such as sickle cell diseases and G6PD deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP526925.RA6ON5nQ96RNQe7LU_n5ZtC9YH-j1L7sb62lQaH0z_Wzw130_provenance.
- NP526925.RA6ON5nQ96RNQe7LU_n5ZtC9YH-j1L7sb62lQaH0z_Wzw130_assertion evidence source_evidence_literature NP526925.RA6ON5nQ96RNQe7LU_n5ZtC9YH-j1L7sb62lQaH0z_Wzw130_provenance.
- NP526925.RA6ON5nQ96RNQe7LU_n5ZtC9YH-j1L7sb62lQaH0z_Wzw130_assertion SIO_000772 16356170 NP526925.RA6ON5nQ96RNQe7LU_n5ZtC9YH-j1L7sb62lQaH0z_Wzw130_provenance.
- NP526925.RA6ON5nQ96RNQe7LU_n5ZtC9YH-j1L7sb62lQaH0z_Wzw130_assertion wasDerivedFrom befree-2016 NP526925.RA6ON5nQ96RNQe7LU_n5ZtC9YH-j1L7sb62lQaH0z_Wzw130_provenance.
- NP526925.RA6ON5nQ96RNQe7LU_n5ZtC9YH-j1L7sb62lQaH0z_Wzw130_assertion wasGeneratedBy ECO_0000203 NP526925.RA6ON5nQ96RNQe7LU_n5ZtC9YH-j1L7sb62lQaH0z_Wzw130_provenance.