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- source_evidence_literature type ECO_0000212 NP526925.RA6ON5nQ96RNQe7LU_n5ZtC9YH-j1L7sb62lQaH0z_Wzw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP526925.RA6ON5nQ96RNQe7LU_n5ZtC9YH-j1L7sb62lQaH0z_Wzw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP526925.RA6ON5nQ96RNQe7LU_n5ZtC9YH-j1L7sb62lQaH0z_Wzw130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP526925.RA6ON5nQ96RNQe7LU_n5ZtC9YH-j1L7sb62lQaH0z_Wzw130_provenance.