Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP77609.RAxcXqESHEXvTH5WJM0kzS6W9oHWRKUpjPZ4edPbD8OUc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP77609.RAxcXqESHEXvTH5WJM0kzS6W9oHWRKUpjPZ4edPbD8OUc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP77609.RAxcXqESHEXvTH5WJM0kzS6W9oHWRKUpjPZ4edPbD8OUc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP77609.RAxcXqESHEXvTH5WJM0kzS6W9oHWRKUpjPZ4edPbD8OUc130_provenance.
- NP77609.RAxcXqESHEXvTH5WJM0kzS6W9oHWRKUpjPZ4edPbD8OUc130_assertion description "[PCR-SSCP analysis of the coding region revealed a single polymorphism in exon 4 leading to an amino acid exchange (G335A; R112H), not significantly associated with either disease. Dinucleotide repeat frequencies of the IL11.A1 allele and of IL11.A1 homozy]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP77609.RAxcXqESHEXvTH5WJM0kzS6W9oHWRKUpjPZ4edPbD8OUc130_provenance.
- NP77609.RAxcXqESHEXvTH5WJM0kzS6W9oHWRKUpjPZ4edPbD8OUc130_assertion evidence source_evidence_literature NP77609.RAxcXqESHEXvTH5WJM0kzS6W9oHWRKUpjPZ4edPbD8OUc130_provenance.
- NP77609.RAxcXqESHEXvTH5WJM0kzS6W9oHWRKUpjPZ4edPbD8OUc130_assertion SIO_000772 12486609 NP77609.RAxcXqESHEXvTH5WJM0kzS6W9oHWRKUpjPZ4edPbD8OUc130_provenance.
- NP77609.RAxcXqESHEXvTH5WJM0kzS6W9oHWRKUpjPZ4edPbD8OUc130_assertion wasDerivedFrom gad-20150221 NP77609.RAxcXqESHEXvTH5WJM0kzS6W9oHWRKUpjPZ4edPbD8OUc130_provenance.
- NP77609.RAxcXqESHEXvTH5WJM0kzS6W9oHWRKUpjPZ4edPbD8OUc130_assertion wasGeneratedBy ECO_0000203 NP77609.RAxcXqESHEXvTH5WJM0kzS6W9oHWRKUpjPZ4edPbD8OUc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP77609.RAxcXqESHEXvTH5WJM0kzS6W9oHWRKUpjPZ4edPbD8OUc130_provenance.