Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP220566.RAT9tGOATYJoDl5i3dw6BSCMwrwIRgv8B97GVUGv9wD0k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP220566.RAT9tGOATYJoDl5i3dw6BSCMwrwIRgv8B97GVUGv9wD0k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP220566.RAT9tGOATYJoDl5i3dw6BSCMwrwIRgv8B97GVUGv9wD0k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP220566.RAT9tGOATYJoDl5i3dw6BSCMwrwIRgv8B97GVUGv9wD0k130_provenance.
- NP220566.RAT9tGOATYJoDl5i3dw6BSCMwrwIRgv8B97GVUGv9wD0k130_assertion description "[An analysis of frequency distribution of the Gln233Arg polymorphism in the leptin receptor gene in children with acute lymphoblastic or acute myeloblastic leukemia showed lack of differences between the patients and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220566.RAT9tGOATYJoDl5i3dw6BSCMwrwIRgv8B97GVUGv9wD0k130_provenance.
- NP220566.RAT9tGOATYJoDl5i3dw6BSCMwrwIRgv8B97GVUGv9wD0k130_assertion evidence source_evidence_literature NP220566.RAT9tGOATYJoDl5i3dw6BSCMwrwIRgv8B97GVUGv9wD0k130_provenance.
- NP220566.RAT9tGOATYJoDl5i3dw6BSCMwrwIRgv8B97GVUGv9wD0k130_assertion SIO_000772 17072067 NP220566.RAT9tGOATYJoDl5i3dw6BSCMwrwIRgv8B97GVUGv9wD0k130_provenance.
- NP220566.RAT9tGOATYJoDl5i3dw6BSCMwrwIRgv8B97GVUGv9wD0k130_assertion wasDerivedFrom lhgdn-20090331 NP220566.RAT9tGOATYJoDl5i3dw6BSCMwrwIRgv8B97GVUGv9wD0k130_provenance.
- NP220566.RAT9tGOATYJoDl5i3dw6BSCMwrwIRgv8B97GVUGv9wD0k130_assertion wasGeneratedBy ECO_0000203 NP220566.RAT9tGOATYJoDl5i3dw6BSCMwrwIRgv8B97GVUGv9wD0k130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP220566.RAT9tGOATYJoDl5i3dw6BSCMwrwIRgv8B97GVUGv9wD0k130_provenance.