Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP643844.RABjmed8aSSvyq12vxPYjT8t9HlvNBnwDgXy_AW7KDW3Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP643844.RABjmed8aSSvyq12vxPYjT8t9HlvNBnwDgXy_AW7KDW3Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP643844.RABjmed8aSSvyq12vxPYjT8t9HlvNBnwDgXy_AW7KDW3Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP643844.RABjmed8aSSvyq12vxPYjT8t9HlvNBnwDgXy_AW7KDW3Q130_provenance.
- NP643844.RABjmed8aSSvyq12vxPYjT8t9HlvNBnwDgXy_AW7KDW3Q130_assertion description "[This is, to the authors' knowledge, the fourth exception to the rule that FAP patients manifesting CHRPE harbour genetic alternations downstream from APC exon 9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP643844.RABjmed8aSSvyq12vxPYjT8t9HlvNBnwDgXy_AW7KDW3Q130_provenance.
- NP643844.RABjmed8aSSvyq12vxPYjT8t9HlvNBnwDgXy_AW7KDW3Q130_assertion evidence source_evidence_literature NP643844.RABjmed8aSSvyq12vxPYjT8t9HlvNBnwDgXy_AW7KDW3Q130_provenance.
- NP643844.RABjmed8aSSvyq12vxPYjT8t9HlvNBnwDgXy_AW7KDW3Q130_assertion SIO_000772 9664575 NP643844.RABjmed8aSSvyq12vxPYjT8t9HlvNBnwDgXy_AW7KDW3Q130_provenance.
- NP643844.RABjmed8aSSvyq12vxPYjT8t9HlvNBnwDgXy_AW7KDW3Q130_assertion wasDerivedFrom befree-20140225 NP643844.RABjmed8aSSvyq12vxPYjT8t9HlvNBnwDgXy_AW7KDW3Q130_provenance.
- NP643844.RABjmed8aSSvyq12vxPYjT8t9HlvNBnwDgXy_AW7KDW3Q130_assertion wasGeneratedBy ECO_0000203 NP643844.RABjmed8aSSvyq12vxPYjT8t9HlvNBnwDgXy_AW7KDW3Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP643844.RABjmed8aSSvyq12vxPYjT8t9HlvNBnwDgXy_AW7KDW3Q130_provenance.