Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP75024.RAFX639T6hYPpnyS8zKssa8it7_3xSdAixtUIQEZHgZlo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP75024.RAFX639T6hYPpnyS8zKssa8it7_3xSdAixtUIQEZHgZlo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP75024.RAFX639T6hYPpnyS8zKssa8it7_3xSdAixtUIQEZHgZlo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP75024.RAFX639T6hYPpnyS8zKssa8it7_3xSdAixtUIQEZHgZlo130_provenance.
- NP75024.RAFX639T6hYPpnyS8zKssa8it7_3xSdAixtUIQEZHgZlo130_assertion description "[ These findings suggest that the TNFR2(+587G) polymorphic allele could be associated with severe CP in Japanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP75024.RAFX639T6hYPpnyS8zKssa8it7_3xSdAixtUIQEZHgZlo130_provenance.
- NP75024.RAFX639T6hYPpnyS8zKssa8it7_3xSdAixtUIQEZHgZlo130_assertion evidence source_evidence_literature NP75024.RAFX639T6hYPpnyS8zKssa8it7_3xSdAixtUIQEZHgZlo130_provenance.
- NP75024.RAFX639T6hYPpnyS8zKssa8it7_3xSdAixtUIQEZHgZlo130_assertion SIO_000772 15142217 NP75024.RAFX639T6hYPpnyS8zKssa8it7_3xSdAixtUIQEZHgZlo130_provenance.
- NP75024.RAFX639T6hYPpnyS8zKssa8it7_3xSdAixtUIQEZHgZlo130_assertion wasDerivedFrom gad-20150221 NP75024.RAFX639T6hYPpnyS8zKssa8it7_3xSdAixtUIQEZHgZlo130_provenance.
- NP75024.RAFX639T6hYPpnyS8zKssa8it7_3xSdAixtUIQEZHgZlo130_assertion wasGeneratedBy ECO_0000203 NP75024.RAFX639T6hYPpnyS8zKssa8it7_3xSdAixtUIQEZHgZlo130_provenance.
- gad-20150221 importedOn "2015-02-21" NP75024.RAFX639T6hYPpnyS8zKssa8it7_3xSdAixtUIQEZHgZlo130_provenance.