Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP179018.RAzMwcB1ZE212mxLYdpaO9_zNZV0XzjjaQa4w9W1PINPI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP179018.RAzMwcB1ZE212mxLYdpaO9_zNZV0XzjjaQa4w9W1PINPI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP179018.RAzMwcB1ZE212mxLYdpaO9_zNZV0XzjjaQa4w9W1PINPI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP179018.RAzMwcB1ZE212mxLYdpaO9_zNZV0XzjjaQa4w9W1PINPI130_provenance.
- NP179018.RAzMwcB1ZE212mxLYdpaO9_zNZV0XzjjaQa4w9W1PINPI130_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." NP179018.RAzMwcB1ZE212mxLYdpaO9_zNZV0XzjjaQa4w9W1PINPI130_provenance.
- NP179018.RAzMwcB1ZE212mxLYdpaO9_zNZV0XzjjaQa4w9W1PINPI130_assertion evidence source_evidence_literature NP179018.RAzMwcB1ZE212mxLYdpaO9_zNZV0XzjjaQa4w9W1PINPI130_provenance.
- NP179018.RAzMwcB1ZE212mxLYdpaO9_zNZV0XzjjaQa4w9W1PINPI130_assertion SIO_000772 7795585 NP179018.RAzMwcB1ZE212mxLYdpaO9_zNZV0XzjjaQa4w9W1PINPI130_provenance.
- NP179018.RAzMwcB1ZE212mxLYdpaO9_zNZV0XzjjaQa4w9W1PINPI130_assertion wasDerivedFrom befree-20140225 NP179018.RAzMwcB1ZE212mxLYdpaO9_zNZV0XzjjaQa4w9W1PINPI130_provenance.
- NP179018.RAzMwcB1ZE212mxLYdpaO9_zNZV0XzjjaQa4w9W1PINPI130_assertion wasGeneratedBy ECO_0000203 NP179018.RAzMwcB1ZE212mxLYdpaO9_zNZV0XzjjaQa4w9W1PINPI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP179018.RAzMwcB1ZE212mxLYdpaO9_zNZV0XzjjaQa4w9W1PINPI130_provenance.