Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP824467.RA71wSD-BCQ3H_vMhbiKWmfimSKNMrb1XWpo_PIn2OBR8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP824467.RA71wSD-BCQ3H_vMhbiKWmfimSKNMrb1XWpo_PIn2OBR8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP824467.RA71wSD-BCQ3H_vMhbiKWmfimSKNMrb1XWpo_PIn2OBR8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP824467.RA71wSD-BCQ3H_vMhbiKWmfimSKNMrb1XWpo_PIn2OBR8130_provenance.
- NP824467.RA71wSD-BCQ3H_vMhbiKWmfimSKNMrb1XWpo_PIn2OBR8130_assertion description "[We investigated a man with a de novo translocation, 46,X,t(Y;3)(p11;p12)dn, who exhibits multiple congenital abnormalities, including severe bilateral VUR with ureterovesical junction defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP824467.RA71wSD-BCQ3H_vMhbiKWmfimSKNMrb1XWpo_PIn2OBR8130_provenance.
- NP824467.RA71wSD-BCQ3H_vMhbiKWmfimSKNMrb1XWpo_PIn2OBR8130_assertion evidence source_evidence_literature NP824467.RA71wSD-BCQ3H_vMhbiKWmfimSKNMrb1XWpo_PIn2OBR8130_provenance.
- NP824467.RA71wSD-BCQ3H_vMhbiKWmfimSKNMrb1XWpo_PIn2OBR8130_assertion SIO_000772 17357069 NP824467.RA71wSD-BCQ3H_vMhbiKWmfimSKNMrb1XWpo_PIn2OBR8130_provenance.
- NP824467.RA71wSD-BCQ3H_vMhbiKWmfimSKNMrb1XWpo_PIn2OBR8130_assertion wasDerivedFrom befree-20140225 NP824467.RA71wSD-BCQ3H_vMhbiKWmfimSKNMrb1XWpo_PIn2OBR8130_provenance.
- NP824467.RA71wSD-BCQ3H_vMhbiKWmfimSKNMrb1XWpo_PIn2OBR8130_assertion wasGeneratedBy ECO_0000203 NP824467.RA71wSD-BCQ3H_vMhbiKWmfimSKNMrb1XWpo_PIn2OBR8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP824467.RA71wSD-BCQ3H_vMhbiKWmfimSKNMrb1XWpo_PIn2OBR8130_provenance.