Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP628129.RAOmIAHBtR2RrL3cC-F_RsfgY_7V5zAjVuubgQ1N8D-IQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP628129.RAOmIAHBtR2RrL3cC-F_RsfgY_7V5zAjVuubgQ1N8D-IQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP628129.RAOmIAHBtR2RrL3cC-F_RsfgY_7V5zAjVuubgQ1N8D-IQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP628129.RAOmIAHBtR2RrL3cC-F_RsfgY_7V5zAjVuubgQ1N8D-IQ130_provenance.
- NP628129.RAOmIAHBtR2RrL3cC-F_RsfgY_7V5zAjVuubgQ1N8D-IQ130_assertion description "[An earlier study has shown that FAP patients with mutations in codons 136-302 of the APC gene do not develop congenital hypertrophy of the retinal pigment epithelium (CHRPE), whereas those with mutations in codons 463-1387 regularly do.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP628129.RAOmIAHBtR2RrL3cC-F_RsfgY_7V5zAjVuubgQ1N8D-IQ130_provenance.
- NP628129.RAOmIAHBtR2RrL3cC-F_RsfgY_7V5zAjVuubgQ1N8D-IQ130_assertion evidence source_evidence_literature NP628129.RAOmIAHBtR2RrL3cC-F_RsfgY_7V5zAjVuubgQ1N8D-IQ130_provenance.
- NP628129.RAOmIAHBtR2RrL3cC-F_RsfgY_7V5zAjVuubgQ1N8D-IQ130_assertion SIO_000772 7795585 NP628129.RAOmIAHBtR2RrL3cC-F_RsfgY_7V5zAjVuubgQ1N8D-IQ130_provenance.
- NP628129.RAOmIAHBtR2RrL3cC-F_RsfgY_7V5zAjVuubgQ1N8D-IQ130_assertion wasDerivedFrom befree-20140225 NP628129.RAOmIAHBtR2RrL3cC-F_RsfgY_7V5zAjVuubgQ1N8D-IQ130_provenance.
- NP628129.RAOmIAHBtR2RrL3cC-F_RsfgY_7V5zAjVuubgQ1N8D-IQ130_assertion wasGeneratedBy ECO_0000203 NP628129.RAOmIAHBtR2RrL3cC-F_RsfgY_7V5zAjVuubgQ1N8D-IQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP628129.RAOmIAHBtR2RrL3cC-F_RsfgY_7V5zAjVuubgQ1N8D-IQ130_provenance.