Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP475892.RABBem7c3jHbYArkeeQFSrKXZH9fIrvvtwUnbcGmd1lj0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP475892.RABBem7c3jHbYArkeeQFSrKXZH9fIrvvtwUnbcGmd1lj0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP475892.RABBem7c3jHbYArkeeQFSrKXZH9fIrvvtwUnbcGmd1lj0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP475892.RABBem7c3jHbYArkeeQFSrKXZH9fIrvvtwUnbcGmd1lj0130_provenance.
- NP475892.RABBem7c3jHbYArkeeQFSrKXZH9fIrvvtwUnbcGmd1lj0130_assertion description "[While the point mutation in Greek HPFH slightly strengthens the binding of CP1 and the CCAAT displacement protein, the same base change strongly reduces the binding of NF-E to the distal CCAAT region, suggesting a possible role of NF-E in the repression of gamma-globin genes in adult erythroid cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475892.RABBem7c3jHbYArkeeQFSrKXZH9fIrvvtwUnbcGmd1lj0130_provenance.
- NP475892.RABBem7c3jHbYArkeeQFSrKXZH9fIrvvtwUnbcGmd1lj0130_assertion evidence source_evidence_literature NP475892.RABBem7c3jHbYArkeeQFSrKXZH9fIrvvtwUnbcGmd1lj0130_provenance.
- NP475892.RABBem7c3jHbYArkeeQFSrKXZH9fIrvvtwUnbcGmd1lj0130_assertion SIO_000772 3181130 NP475892.RABBem7c3jHbYArkeeQFSrKXZH9fIrvvtwUnbcGmd1lj0130_provenance.
- NP475892.RABBem7c3jHbYArkeeQFSrKXZH9fIrvvtwUnbcGmd1lj0130_assertion wasDerivedFrom befree-20140225 NP475892.RABBem7c3jHbYArkeeQFSrKXZH9fIrvvtwUnbcGmd1lj0130_provenance.
- NP475892.RABBem7c3jHbYArkeeQFSrKXZH9fIrvvtwUnbcGmd1lj0130_assertion wasGeneratedBy ECO_0000203 NP475892.RABBem7c3jHbYArkeeQFSrKXZH9fIrvvtwUnbcGmd1lj0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP475892.RABBem7c3jHbYArkeeQFSrKXZH9fIrvvtwUnbcGmd1lj0130_provenance.