Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP210775.RA4Ig9BIwIefO8rctlJ-_i5DimVwB1cyASeWdjH-H5PIY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP210775.RA4Ig9BIwIefO8rctlJ-_i5DimVwB1cyASeWdjH-H5PIY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP210775.RA4Ig9BIwIefO8rctlJ-_i5DimVwB1cyASeWdjH-H5PIY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP210775.RA4Ig9BIwIefO8rctlJ-_i5DimVwB1cyASeWdjH-H5PIY130_provenance.
- NP210775.RA4Ig9BIwIefO8rctlJ-_i5DimVwB1cyASeWdjH-H5PIY130_assertion description "[Sequencing of the entire coding region and splice junctions of AKT2 and the relationship of genetic variations in the gene with multiple metabolic diseases is reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210775.RA4Ig9BIwIefO8rctlJ-_i5DimVwB1cyASeWdjH-H5PIY130_provenance.
- NP210775.RA4Ig9BIwIefO8rctlJ-_i5DimVwB1cyASeWdjH-H5PIY130_assertion evidence source_evidence_literature NP210775.RA4Ig9BIwIefO8rctlJ-_i5DimVwB1cyASeWdjH-H5PIY130_provenance.
- NP210775.RA4Ig9BIwIefO8rctlJ-_i5DimVwB1cyASeWdjH-H5PIY130_assertion SIO_000772 17327441 NP210775.RA4Ig9BIwIefO8rctlJ-_i5DimVwB1cyASeWdjH-H5PIY130_provenance.
- NP210775.RA4Ig9BIwIefO8rctlJ-_i5DimVwB1cyASeWdjH-H5PIY130_assertion wasDerivedFrom lhgdn-20090331 NP210775.RA4Ig9BIwIefO8rctlJ-_i5DimVwB1cyASeWdjH-H5PIY130_provenance.
- NP210775.RA4Ig9BIwIefO8rctlJ-_i5DimVwB1cyASeWdjH-H5PIY130_assertion wasGeneratedBy ECO_0000203 NP210775.RA4Ig9BIwIefO8rctlJ-_i5DimVwB1cyASeWdjH-H5PIY130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP210775.RA4Ig9BIwIefO8rctlJ-_i5DimVwB1cyASeWdjH-H5PIY130_provenance.