Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP86205.RAKK8860zqMWQaw5R6NCNsGkGeQLAgCtCVBk4DwO2_7n8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP86205.RAKK8860zqMWQaw5R6NCNsGkGeQLAgCtCVBk4DwO2_7n8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP86205.RAKK8860zqMWQaw5R6NCNsGkGeQLAgCtCVBk4DwO2_7n8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP86205.RAKK8860zqMWQaw5R6NCNsGkGeQLAgCtCVBk4DwO2_7n8130_provenance.
- NP86205.RAKK8860zqMWQaw5R6NCNsGkGeQLAgCtCVBk4DwO2_7n8130_assertion description "[Examination of genetic polymorphisms in newborns for signatures of sex-specific prenatal selection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP86205.RAKK8860zqMWQaw5R6NCNsGkGeQLAgCtCVBk4DwO2_7n8130_provenance.
- NP86205.RAKK8860zqMWQaw5R6NCNsGkGeQLAgCtCVBk4DwO2_7n8130_assertion evidence source_evidence_literature NP86205.RAKK8860zqMWQaw5R6NCNsGkGeQLAgCtCVBk4DwO2_7n8130_provenance.
- NP86205.RAKK8860zqMWQaw5R6NCNsGkGeQLAgCtCVBk4DwO2_7n8130_assertion SIO_000772 20587610 NP86205.RAKK8860zqMWQaw5R6NCNsGkGeQLAgCtCVBk4DwO2_7n8130_provenance.
- NP86205.RAKK8860zqMWQaw5R6NCNsGkGeQLAgCtCVBk4DwO2_7n8130_assertion wasDerivedFrom gad-20130706 NP86205.RAKK8860zqMWQaw5R6NCNsGkGeQLAgCtCVBk4DwO2_7n8130_provenance.
- NP86205.RAKK8860zqMWQaw5R6NCNsGkGeQLAgCtCVBk4DwO2_7n8130_assertion wasGeneratedBy ECO_0000203 NP86205.RAKK8860zqMWQaw5R6NCNsGkGeQLAgCtCVBk4DwO2_7n8130_provenance.
- gad-20130706 importedOn "2013-07-06" NP86205.RAKK8860zqMWQaw5R6NCNsGkGeQLAgCtCVBk4DwO2_7n8130_provenance.