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- NP480899.RA91hCJy5-XwEU9Rl8GN7Z9tbkR_9qOL2bvHySQAES0I0130_assertion type Assertion NP480899.RA91hCJy5-XwEU9Rl8GN7Z9tbkR_9qOL2bvHySQAES0I0130_head.
- NP480899.RA91hCJy5-XwEU9Rl8GN7Z9tbkR_9qOL2bvHySQAES0I0130_assertion wasGeneratedBy ECO_0000203 NP480899.RA91hCJy5-XwEU9Rl8GN7Z9tbkR_9qOL2bvHySQAES0I0130_provenance.
- NP480899.RA91hCJy5-XwEU9Rl8GN7Z9tbkR_9qOL2bvHySQAES0I0130_assertion wasDerivedFrom befree-20140225 NP480899.RA91hCJy5-XwEU9Rl8GN7Z9tbkR_9qOL2bvHySQAES0I0130_provenance.
- NP480899.RA91hCJy5-XwEU9Rl8GN7Z9tbkR_9qOL2bvHySQAES0I0130_assertion SIO_000772 22509377 NP480899.RA91hCJy5-XwEU9Rl8GN7Z9tbkR_9qOL2bvHySQAES0I0130_provenance.
- NP480899.RA91hCJy5-XwEU9Rl8GN7Z9tbkR_9qOL2bvHySQAES0I0130_assertion evidence source_evidence_literature NP480899.RA91hCJy5-XwEU9Rl8GN7Z9tbkR_9qOL2bvHySQAES0I0130_provenance.
- NP480899.RA91hCJy5-XwEU9Rl8GN7Z9tbkR_9qOL2bvHySQAES0I0130_assertion description "[Candidate gene sequencing of SLC11A2 and TMPRSS6 in a family with severe anaemia: common SNPs, rare haplotypes, no causative mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP480899.RA91hCJy5-XwEU9Rl8GN7Z9tbkR_9qOL2bvHySQAES0I0130_provenance.