Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP532339.RANNZKOxnwa8zkZ_csKqn8erspGQ6G1baC7W_grApXDG8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP532339.RANNZKOxnwa8zkZ_csKqn8erspGQ6G1baC7W_grApXDG8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP532339.RANNZKOxnwa8zkZ_csKqn8erspGQ6G1baC7W_grApXDG8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP532339.RANNZKOxnwa8zkZ_csKqn8erspGQ6G1baC7W_grApXDG8130_provenance.
- NP532339.RANNZKOxnwa8zkZ_csKqn8erspGQ6G1baC7W_grApXDG8130_assertion description "[Heterozygosity for this postulated mutation (father of the patients with thalassaemia intermedia) may result in the production of a beta-thalassaemia carrier state with normal HbA2 level.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532339.RANNZKOxnwa8zkZ_csKqn8erspGQ6G1baC7W_grApXDG8130_provenance.
- NP532339.RANNZKOxnwa8zkZ_csKqn8erspGQ6G1baC7W_grApXDG8130_assertion evidence source_evidence_literature NP532339.RANNZKOxnwa8zkZ_csKqn8erspGQ6G1baC7W_grApXDG8130_provenance.
- NP532339.RANNZKOxnwa8zkZ_csKqn8erspGQ6G1baC7W_grApXDG8130_assertion SIO_000772 1643026 NP532339.RANNZKOxnwa8zkZ_csKqn8erspGQ6G1baC7W_grApXDG8130_provenance.
- NP532339.RANNZKOxnwa8zkZ_csKqn8erspGQ6G1baC7W_grApXDG8130_assertion wasDerivedFrom befree-2016 NP532339.RANNZKOxnwa8zkZ_csKqn8erspGQ6G1baC7W_grApXDG8130_provenance.
- NP532339.RANNZKOxnwa8zkZ_csKqn8erspGQ6G1baC7W_grApXDG8130_assertion wasGeneratedBy ECO_0000203 NP532339.RANNZKOxnwa8zkZ_csKqn8erspGQ6G1baC7W_grApXDG8130_provenance.
- befree-2016 importedOn "2016-02-19" NP532339.RANNZKOxnwa8zkZ_csKqn8erspGQ6G1baC7W_grApXDG8130_provenance.