Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP540824.RAxe_5M7ILkdq-gqQOj3x7vRI0EB59bSrUtiCNP9LzBec130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP540824.RAxe_5M7ILkdq-gqQOj3x7vRI0EB59bSrUtiCNP9LzBec130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP540824.RAxe_5M7ILkdq-gqQOj3x7vRI0EB59bSrUtiCNP9LzBec130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP540824.RAxe_5M7ILkdq-gqQOj3x7vRI0EB59bSrUtiCNP9LzBec130_provenance.
- NP540824.RAxe_5M7ILkdq-gqQOj3x7vRI0EB59bSrUtiCNP9LzBec130_assertion description "[The Hp phenotype distribution resulted in allele frequencies of 0 625 (Hp(2)), 0.281 (Hp(1S)), and 0.093 (Hp(1F)) in healthy controls, correlating fairly well with the allele frequencies of European populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP540824.RAxe_5M7ILkdq-gqQOj3x7vRI0EB59bSrUtiCNP9LzBec130_provenance.
- NP540824.RAxe_5M7ILkdq-gqQOj3x7vRI0EB59bSrUtiCNP9LzBec130_assertion evidence source_evidence_literature NP540824.RAxe_5M7ILkdq-gqQOj3x7vRI0EB59bSrUtiCNP9LzBec130_provenance.
- NP540824.RAxe_5M7ILkdq-gqQOj3x7vRI0EB59bSrUtiCNP9LzBec130_assertion SIO_000772 16544281 NP540824.RAxe_5M7ILkdq-gqQOj3x7vRI0EB59bSrUtiCNP9LzBec130_provenance.
- NP540824.RAxe_5M7ILkdq-gqQOj3x7vRI0EB59bSrUtiCNP9LzBec130_assertion wasDerivedFrom befree-2016 NP540824.RAxe_5M7ILkdq-gqQOj3x7vRI0EB59bSrUtiCNP9LzBec130_provenance.
- NP540824.RAxe_5M7ILkdq-gqQOj3x7vRI0EB59bSrUtiCNP9LzBec130_assertion wasGeneratedBy ECO_0000203 NP540824.RAxe_5M7ILkdq-gqQOj3x7vRI0EB59bSrUtiCNP9LzBec130_provenance.
- befree-2016 importedOn "2016-02-19" NP540824.RAxe_5M7ILkdq-gqQOj3x7vRI0EB59bSrUtiCNP9LzBec130_provenance.