Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP519233.RA3oSWEPPyNEif8-lDGIo44rLzf5TbryrdMFX1xkwfbkA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP519233.RA3oSWEPPyNEif8-lDGIo44rLzf5TbryrdMFX1xkwfbkA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP519233.RA3oSWEPPyNEif8-lDGIo44rLzf5TbryrdMFX1xkwfbkA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP519233.RA3oSWEPPyNEif8-lDGIo44rLzf5TbryrdMFX1xkwfbkA130_provenance.
- NP519233.RA3oSWEPPyNEif8-lDGIo44rLzf5TbryrdMFX1xkwfbkA130_assertion description "[We have determined the frequencies of the A and G alleles of the HOXA1 A218G polymorphism in both white and black patients from the South Carolina Autism Project (SCAP) and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519233.RA3oSWEPPyNEif8-lDGIo44rLzf5TbryrdMFX1xkwfbkA130_provenance.
- NP519233.RA3oSWEPPyNEif8-lDGIo44rLzf5TbryrdMFX1xkwfbkA130_assertion evidence source_evidence_literature NP519233.RA3oSWEPPyNEif8-lDGIo44rLzf5TbryrdMFX1xkwfbkA130_provenance.
- NP519233.RA3oSWEPPyNEif8-lDGIo44rLzf5TbryrdMFX1xkwfbkA130_assertion SIO_000772 12908836 NP519233.RA3oSWEPPyNEif8-lDGIo44rLzf5TbryrdMFX1xkwfbkA130_provenance.
- NP519233.RA3oSWEPPyNEif8-lDGIo44rLzf5TbryrdMFX1xkwfbkA130_assertion wasDerivedFrom befree-20140225 NP519233.RA3oSWEPPyNEif8-lDGIo44rLzf5TbryrdMFX1xkwfbkA130_provenance.
- NP519233.RA3oSWEPPyNEif8-lDGIo44rLzf5TbryrdMFX1xkwfbkA130_assertion wasGeneratedBy ECO_0000203 NP519233.RA3oSWEPPyNEif8-lDGIo44rLzf5TbryrdMFX1xkwfbkA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP519233.RA3oSWEPPyNEif8-lDGIo44rLzf5TbryrdMFX1xkwfbkA130_provenance.