Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP85058.RAWI2lzATFWHGi5I12aJChqOCes3CS0_Fvlq20iNnWWHg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP85058.RAWI2lzATFWHGi5I12aJChqOCes3CS0_Fvlq20iNnWWHg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP85058.RAWI2lzATFWHGi5I12aJChqOCes3CS0_Fvlq20iNnWWHg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP85058.RAWI2lzATFWHGi5I12aJChqOCes3CS0_Fvlq20iNnWWHg130_provenance.
- NP85058.RAWI2lzATFWHGi5I12aJChqOCes3CS0_Fvlq20iNnWWHg130_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." NP85058.RAWI2lzATFWHGi5I12aJChqOCes3CS0_Fvlq20iNnWWHg130_provenance.
- NP85058.RAWI2lzATFWHGi5I12aJChqOCes3CS0_Fvlq20iNnWWHg130_assertion evidence source_evidence_literature NP85058.RAWI2lzATFWHGi5I12aJChqOCes3CS0_Fvlq20iNnWWHg130_provenance.
- NP85058.RAWI2lzATFWHGi5I12aJChqOCes3CS0_Fvlq20iNnWWHg130_assertion SIO_000772 20587610 NP85058.RAWI2lzATFWHGi5I12aJChqOCes3CS0_Fvlq20iNnWWHg130_provenance.
- NP85058.RAWI2lzATFWHGi5I12aJChqOCes3CS0_Fvlq20iNnWWHg130_assertion wasDerivedFrom gad-20130706 NP85058.RAWI2lzATFWHGi5I12aJChqOCes3CS0_Fvlq20iNnWWHg130_provenance.
- NP85058.RAWI2lzATFWHGi5I12aJChqOCes3CS0_Fvlq20iNnWWHg130_assertion wasGeneratedBy ECO_0000203 NP85058.RAWI2lzATFWHGi5I12aJChqOCes3CS0_Fvlq20iNnWWHg130_provenance.
- gad-20130706 importedOn "2013-07-06" NP85058.RAWI2lzATFWHGi5I12aJChqOCes3CS0_Fvlq20iNnWWHg130_provenance.