Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP945135.RAK9RVOY1DwR3y2awq5igkvlxRU14B6inqb5akumqDkGo130_assertion> ?p ?o ?g. }
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- NP945135.RAK9RVOY1DwR3y2awq5igkvlxRU14B6inqb5akumqDkGo130_assertion type Assertion NP945135.RAK9RVOY1DwR3y2awq5igkvlxRU14B6inqb5akumqDkGo130_head.
- NP945135.RAK9RVOY1DwR3y2awq5igkvlxRU14B6inqb5akumqDkGo130_assertion wasGeneratedBy ECO_0000203 NP945135.RAK9RVOY1DwR3y2awq5igkvlxRU14B6inqb5akumqDkGo130_provenance.
- NP945135.RAK9RVOY1DwR3y2awq5igkvlxRU14B6inqb5akumqDkGo130_assertion wasDerivedFrom befree-20150227 NP945135.RAK9RVOY1DwR3y2awq5igkvlxRU14B6inqb5akumqDkGo130_provenance.
- NP945135.RAK9RVOY1DwR3y2awq5igkvlxRU14B6inqb5akumqDkGo130_assertion SIO_000772 22461326 NP945135.RAK9RVOY1DwR3y2awq5igkvlxRU14B6inqb5akumqDkGo130_provenance.
- NP945135.RAK9RVOY1DwR3y2awq5igkvlxRU14B6inqb5akumqDkGo130_assertion evidence source_evidence_literature NP945135.RAK9RVOY1DwR3y2awq5igkvlxRU14B6inqb5akumqDkGo130_provenance.
- NP945135.RAK9RVOY1DwR3y2awq5igkvlxRU14B6inqb5akumqDkGo130_assertion description "[Although this study does not provide irrefutable evidence that GALNT12 variants are highly penetrant alleles that predispose to CRC in the majority of unexplained hereditary CRC families, it does provide additional evidence to support an important role of these variants in a proportion of this considerable high-risk group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP945135.RAK9RVOY1DwR3y2awq5igkvlxRU14B6inqb5akumqDkGo130_provenance.