Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP159730.RAdA_VN9Qs2-P8EBKO38oaFdw6WbeFHO2uiObmvXj-DEg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP159730.RAdA_VN9Qs2-P8EBKO38oaFdw6WbeFHO2uiObmvXj-DEg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP159730.RAdA_VN9Qs2-P8EBKO38oaFdw6WbeFHO2uiObmvXj-DEg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP159730.RAdA_VN9Qs2-P8EBKO38oaFdw6WbeFHO2uiObmvXj-DEg130_provenance.
- NP159730.RAdA_VN9Qs2-P8EBKO38oaFdw6WbeFHO2uiObmvXj-DEg130_assertion description "[Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP159730.RAdA_VN9Qs2-P8EBKO38oaFdw6WbeFHO2uiObmvXj-DEg130_provenance.
- NP159730.RAdA_VN9Qs2-P8EBKO38oaFdw6WbeFHO2uiObmvXj-DEg130_assertion evidence source_evidence_literature NP159730.RAdA_VN9Qs2-P8EBKO38oaFdw6WbeFHO2uiObmvXj-DEg130_provenance.
- NP159730.RAdA_VN9Qs2-P8EBKO38oaFdw6WbeFHO2uiObmvXj-DEg130_assertion SIO_000772 21901158 NP159730.RAdA_VN9Qs2-P8EBKO38oaFdw6WbeFHO2uiObmvXj-DEg130_provenance.
- NP159730.RAdA_VN9Qs2-P8EBKO38oaFdw6WbeFHO2uiObmvXj-DEg130_assertion wasDerivedFrom gad-20150221 NP159730.RAdA_VN9Qs2-P8EBKO38oaFdw6WbeFHO2uiObmvXj-DEg130_provenance.
- NP159730.RAdA_VN9Qs2-P8EBKO38oaFdw6WbeFHO2uiObmvXj-DEg130_assertion wasGeneratedBy ECO_0000203 NP159730.RAdA_VN9Qs2-P8EBKO38oaFdw6WbeFHO2uiObmvXj-DEg130_provenance.
- gad-20150221 importedOn "2015-02-21" NP159730.RAdA_VN9Qs2-P8EBKO38oaFdw6WbeFHO2uiObmvXj-DEg130_provenance.