Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP925849.RAUZshfPTPkgQLcJnD01kM_rFCLkmYSmMDK6AuX5qf-Ws130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP925849.RAUZshfPTPkgQLcJnD01kM_rFCLkmYSmMDK6AuX5qf-Ws130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925849.RAUZshfPTPkgQLcJnD01kM_rFCLkmYSmMDK6AuX5qf-Ws130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925849.RAUZshfPTPkgQLcJnD01kM_rFCLkmYSmMDK6AuX5qf-Ws130_provenance.
- NP925849.RAUZshfPTPkgQLcJnD01kM_rFCLkmYSmMDK6AuX5qf-Ws130_assertion wasGeneratedBy ECO_0000203 NP925849.RAUZshfPTPkgQLcJnD01kM_rFCLkmYSmMDK6AuX5qf-Ws130_provenance.
- NP925849.RAUZshfPTPkgQLcJnD01kM_rFCLkmYSmMDK6AuX5qf-Ws130_assertion wasDerivedFrom befree-20140225 NP925849.RAUZshfPTPkgQLcJnD01kM_rFCLkmYSmMDK6AuX5qf-Ws130_provenance.
- NP925849.RAUZshfPTPkgQLcJnD01kM_rFCLkmYSmMDK6AuX5qf-Ws130_assertion SIO_000772 22461326 NP925849.RAUZshfPTPkgQLcJnD01kM_rFCLkmYSmMDK6AuX5qf-Ws130_provenance.
- NP925849.RAUZshfPTPkgQLcJnD01kM_rFCLkmYSmMDK6AuX5qf-Ws130_assertion evidence source_evidence_literature NP925849.RAUZshfPTPkgQLcJnD01kM_rFCLkmYSmMDK6AuX5qf-Ws130_provenance.
- NP925849.RAUZshfPTPkgQLcJnD01kM_rFCLkmYSmMDK6AuX5qf-Ws130_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." NP925849.RAUZshfPTPkgQLcJnD01kM_rFCLkmYSmMDK6AuX5qf-Ws130_provenance.
- befree-20140225 importedOn "2014-02-25" NP925849.RAUZshfPTPkgQLcJnD01kM_rFCLkmYSmMDK6AuX5qf-Ws130_provenance.