Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP888428.RAlaPHL6k3xtoHRmFHLm7TY5pTxOBO26-MxIg_lpzjZfU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP888428.RAlaPHL6k3xtoHRmFHLm7TY5pTxOBO26-MxIg_lpzjZfU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP888428.RAlaPHL6k3xtoHRmFHLm7TY5pTxOBO26-MxIg_lpzjZfU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP888428.RAlaPHL6k3xtoHRmFHLm7TY5pTxOBO26-MxIg_lpzjZfU130_provenance.
- NP888428.RAlaPHL6k3xtoHRmFHLm7TY5pTxOBO26-MxIg_lpzjZfU130_assertion description "[MAP phenotype is similar to the FAP phenotype because of the somatic mutations to the APC gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP888428.RAlaPHL6k3xtoHRmFHLm7TY5pTxOBO26-MxIg_lpzjZfU130_provenance.
- NP888428.RAlaPHL6k3xtoHRmFHLm7TY5pTxOBO26-MxIg_lpzjZfU130_assertion evidence source_evidence_literature NP888428.RAlaPHL6k3xtoHRmFHLm7TY5pTxOBO26-MxIg_lpzjZfU130_provenance.
- NP888428.RAlaPHL6k3xtoHRmFHLm7TY5pTxOBO26-MxIg_lpzjZfU130_assertion SIO_000772 21505584 NP888428.RAlaPHL6k3xtoHRmFHLm7TY5pTxOBO26-MxIg_lpzjZfU130_provenance.
- NP888428.RAlaPHL6k3xtoHRmFHLm7TY5pTxOBO26-MxIg_lpzjZfU130_assertion wasDerivedFrom befree-2016 NP888428.RAlaPHL6k3xtoHRmFHLm7TY5pTxOBO26-MxIg_lpzjZfU130_provenance.
- NP888428.RAlaPHL6k3xtoHRmFHLm7TY5pTxOBO26-MxIg_lpzjZfU130_assertion wasGeneratedBy ECO_0000203 NP888428.RAlaPHL6k3xtoHRmFHLm7TY5pTxOBO26-MxIg_lpzjZfU130_provenance.
- befree-2016 importedOn "2016-02-19" NP888428.RAlaPHL6k3xtoHRmFHLm7TY5pTxOBO26-MxIg_lpzjZfU130_provenance.