Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP816242.RAWP2NDFkcM7n7Cqa1oqAeuG3vS4e7ZEDaqqT-wSlTssU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP816242.RAWP2NDFkcM7n7Cqa1oqAeuG3vS4e7ZEDaqqT-wSlTssU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP816242.RAWP2NDFkcM7n7Cqa1oqAeuG3vS4e7ZEDaqqT-wSlTssU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP816242.RAWP2NDFkcM7n7Cqa1oqAeuG3vS4e7ZEDaqqT-wSlTssU130_provenance.
- NP816242.RAWP2NDFkcM7n7Cqa1oqAeuG3vS4e7ZEDaqqT-wSlTssU130_assertion description "[We evaluated a series of European CRC patients and population controls to clarify whether EXO1 variants may indeed predispose to familial CRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP816242.RAWP2NDFkcM7n7Cqa1oqAeuG3vS4e7ZEDaqqT-wSlTssU130_provenance.
- NP816242.RAWP2NDFkcM7n7Cqa1oqAeuG3vS4e7ZEDaqqT-wSlTssU130_assertion evidence source_evidence_literature NP816242.RAWP2NDFkcM7n7Cqa1oqAeuG3vS4e7ZEDaqqT-wSlTssU130_provenance.
- NP816242.RAWP2NDFkcM7n7Cqa1oqAeuG3vS4e7ZEDaqqT-wSlTssU130_assertion SIO_000772 12517792 NP816242.RAWP2NDFkcM7n7Cqa1oqAeuG3vS4e7ZEDaqqT-wSlTssU130_provenance.
- NP816242.RAWP2NDFkcM7n7Cqa1oqAeuG3vS4e7ZEDaqqT-wSlTssU130_assertion wasDerivedFrom befree-20150227 NP816242.RAWP2NDFkcM7n7Cqa1oqAeuG3vS4e7ZEDaqqT-wSlTssU130_provenance.
- NP816242.RAWP2NDFkcM7n7Cqa1oqAeuG3vS4e7ZEDaqqT-wSlTssU130_assertion wasGeneratedBy ECO_0000203 NP816242.RAWP2NDFkcM7n7Cqa1oqAeuG3vS4e7ZEDaqqT-wSlTssU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP816242.RAWP2NDFkcM7n7Cqa1oqAeuG3vS4e7ZEDaqqT-wSlTssU130_provenance.