Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP922021.RAd0jJBVI16CalpwnXpEFzFFeWoF2MwBVZ-AEUU5IAOTs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP922021.RAd0jJBVI16CalpwnXpEFzFFeWoF2MwBVZ-AEUU5IAOTs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP922021.RAd0jJBVI16CalpwnXpEFzFFeWoF2MwBVZ-AEUU5IAOTs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP922021.RAd0jJBVI16CalpwnXpEFzFFeWoF2MwBVZ-AEUU5IAOTs130_provenance.
- NP922021.RAd0jJBVI16CalpwnXpEFzFFeWoF2MwBVZ-AEUU5IAOTs130_assertion description "[The linkage between mutations and clinical and pathologic outcomes was interrogated with the Fisher exact test (for stage and Fuhrman nuclear grade) and the permutation log-rank test (for cancer-specific survival [CSS]).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP922021.RAd0jJBVI16CalpwnXpEFzFFeWoF2MwBVZ-AEUU5IAOTs130_provenance.
- NP922021.RAd0jJBVI16CalpwnXpEFzFFeWoF2MwBVZ-AEUU5IAOTs130_assertion evidence source_evidence_literature NP922021.RAd0jJBVI16CalpwnXpEFzFFeWoF2MwBVZ-AEUU5IAOTs130_provenance.
- NP922021.RAd0jJBVI16CalpwnXpEFzFFeWoF2MwBVZ-AEUU5IAOTs130_assertion SIO_000772 23036577 NP922021.RAd0jJBVI16CalpwnXpEFzFFeWoF2MwBVZ-AEUU5IAOTs130_provenance.
- NP922021.RAd0jJBVI16CalpwnXpEFzFFeWoF2MwBVZ-AEUU5IAOTs130_assertion wasDerivedFrom befree-20150227 NP922021.RAd0jJBVI16CalpwnXpEFzFFeWoF2MwBVZ-AEUU5IAOTs130_provenance.
- NP922021.RAd0jJBVI16CalpwnXpEFzFFeWoF2MwBVZ-AEUU5IAOTs130_assertion wasGeneratedBy ECO_0000203 NP922021.RAd0jJBVI16CalpwnXpEFzFFeWoF2MwBVZ-AEUU5IAOTs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP922021.RAd0jJBVI16CalpwnXpEFzFFeWoF2MwBVZ-AEUU5IAOTs130_provenance.