Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP975448.RAKCsMLLdgaSK7kQK3DDLJFYcf2CZmvGrnGCAW0N3fJVE130_assertion> ?p ?o ?g. }
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- NP975448.RAKCsMLLdgaSK7kQK3DDLJFYcf2CZmvGrnGCAW0N3fJVE130_assertion type Assertion NP975448.RAKCsMLLdgaSK7kQK3DDLJFYcf2CZmvGrnGCAW0N3fJVE130_head.
- NP975448.RAKCsMLLdgaSK7kQK3DDLJFYcf2CZmvGrnGCAW0N3fJVE130_assertion wasGeneratedBy ECO_0000203 NP975448.RAKCsMLLdgaSK7kQK3DDLJFYcf2CZmvGrnGCAW0N3fJVE130_provenance.
- NP975448.RAKCsMLLdgaSK7kQK3DDLJFYcf2CZmvGrnGCAW0N3fJVE130_assertion wasDerivedFrom befree-2016 NP975448.RAKCsMLLdgaSK7kQK3DDLJFYcf2CZmvGrnGCAW0N3fJVE130_provenance.
- NP975448.RAKCsMLLdgaSK7kQK3DDLJFYcf2CZmvGrnGCAW0N3fJVE130_assertion SIO_000772 22509377 NP975448.RAKCsMLLdgaSK7kQK3DDLJFYcf2CZmvGrnGCAW0N3fJVE130_provenance.
- NP975448.RAKCsMLLdgaSK7kQK3DDLJFYcf2CZmvGrnGCAW0N3fJVE130_assertion evidence source_evidence_literature NP975448.RAKCsMLLdgaSK7kQK3DDLJFYcf2CZmvGrnGCAW0N3fJVE130_provenance.
- NP975448.RAKCsMLLdgaSK7kQK3DDLJFYcf2CZmvGrnGCAW0N3fJVE130_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." NP975448.RAKCsMLLdgaSK7kQK3DDLJFYcf2CZmvGrnGCAW0N3fJVE130_provenance.