Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP444075.RANGo7kvTHtLlAMATmNREWSBSwzQ4uUom2Br8rT4g40xY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP444075.RANGo7kvTHtLlAMATmNREWSBSwzQ4uUom2Br8rT4g40xY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP444075.RANGo7kvTHtLlAMATmNREWSBSwzQ4uUom2Br8rT4g40xY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP444075.RANGo7kvTHtLlAMATmNREWSBSwzQ4uUom2Br8rT4g40xY130_provenance.
- NP444075.RANGo7kvTHtLlAMATmNREWSBSwzQ4uUom2Br8rT4g40xY130_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." NP444075.RANGo7kvTHtLlAMATmNREWSBSwzQ4uUom2Br8rT4g40xY130_provenance.
- NP444075.RANGo7kvTHtLlAMATmNREWSBSwzQ4uUom2Br8rT4g40xY130_assertion evidence source_evidence_literature NP444075.RANGo7kvTHtLlAMATmNREWSBSwzQ4uUom2Br8rT4g40xY130_provenance.
- NP444075.RANGo7kvTHtLlAMATmNREWSBSwzQ4uUom2Br8rT4g40xY130_assertion SIO_000772 15142217 NP444075.RANGo7kvTHtLlAMATmNREWSBSwzQ4uUom2Br8rT4g40xY130_provenance.
- NP444075.RANGo7kvTHtLlAMATmNREWSBSwzQ4uUom2Br8rT4g40xY130_assertion wasDerivedFrom befree-2016 NP444075.RANGo7kvTHtLlAMATmNREWSBSwzQ4uUom2Br8rT4g40xY130_provenance.
- NP444075.RANGo7kvTHtLlAMATmNREWSBSwzQ4uUom2Br8rT4g40xY130_assertion wasGeneratedBy ECO_0000203 NP444075.RANGo7kvTHtLlAMATmNREWSBSwzQ4uUom2Br8rT4g40xY130_provenance.
- befree-2016 importedOn "2016-02-19" NP444075.RANGo7kvTHtLlAMATmNREWSBSwzQ4uUom2Br8rT4g40xY130_provenance.