Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP812609.RAEfHSflkhnmOdg3O4SUXoFXLNLsmcAwphcszFbobWmbo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP812609.RAEfHSflkhnmOdg3O4SUXoFXLNLsmcAwphcszFbobWmbo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP812609.RAEfHSflkhnmOdg3O4SUXoFXLNLsmcAwphcszFbobWmbo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP812609.RAEfHSflkhnmOdg3O4SUXoFXLNLsmcAwphcszFbobWmbo130_provenance.
- NP812609.RAEfHSflkhnmOdg3O4SUXoFXLNLsmcAwphcszFbobWmbo130_assertion description "[Amniocentesis on a 32-year-old woman at risk for trisomy 21 by maternal serum triple screen showed a 46,Y,inv(X) (p22.1q24) karyotype in all cells analyzed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP812609.RAEfHSflkhnmOdg3O4SUXoFXLNLsmcAwphcszFbobWmbo130_provenance.
- NP812609.RAEfHSflkhnmOdg3O4SUXoFXLNLsmcAwphcszFbobWmbo130_assertion evidence source_evidence_literature NP812609.RAEfHSflkhnmOdg3O4SUXoFXLNLsmcAwphcszFbobWmbo130_provenance.
- NP812609.RAEfHSflkhnmOdg3O4SUXoFXLNLsmcAwphcszFbobWmbo130_assertion SIO_000772 10588841 NP812609.RAEfHSflkhnmOdg3O4SUXoFXLNLsmcAwphcszFbobWmbo130_provenance.
- NP812609.RAEfHSflkhnmOdg3O4SUXoFXLNLsmcAwphcszFbobWmbo130_assertion wasDerivedFrom befree-20140225 NP812609.RAEfHSflkhnmOdg3O4SUXoFXLNLsmcAwphcszFbobWmbo130_provenance.
- NP812609.RAEfHSflkhnmOdg3O4SUXoFXLNLsmcAwphcszFbobWmbo130_assertion wasGeneratedBy ECO_0000203 NP812609.RAEfHSflkhnmOdg3O4SUXoFXLNLsmcAwphcszFbobWmbo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP812609.RAEfHSflkhnmOdg3O4SUXoFXLNLsmcAwphcszFbobWmbo130_provenance.