Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP574584.RA1DgwVwTj9vTWsTZFduj9_EAc_MkJw2DQKrJAKVwqm_k130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP574584.RA1DgwVwTj9vTWsTZFduj9_EAc_MkJw2DQKrJAKVwqm_k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP574584.RA1DgwVwTj9vTWsTZFduj9_EAc_MkJw2DQKrJAKVwqm_k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP574584.RA1DgwVwTj9vTWsTZFduj9_EAc_MkJw2DQKrJAKVwqm_k130_provenance.
- NP574584.RA1DgwVwTj9vTWsTZFduj9_EAc_MkJw2DQKrJAKVwqm_k130_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." NP574584.RA1DgwVwTj9vTWsTZFduj9_EAc_MkJw2DQKrJAKVwqm_k130_provenance.
- NP574584.RA1DgwVwTj9vTWsTZFduj9_EAc_MkJw2DQKrJAKVwqm_k130_assertion evidence source_evidence_literature NP574584.RA1DgwVwTj9vTWsTZFduj9_EAc_MkJw2DQKrJAKVwqm_k130_provenance.
- NP574584.RA1DgwVwTj9vTWsTZFduj9_EAc_MkJw2DQKrJAKVwqm_k130_assertion SIO_000772 7795585 NP574584.RA1DgwVwTj9vTWsTZFduj9_EAc_MkJw2DQKrJAKVwqm_k130_provenance.
- NP574584.RA1DgwVwTj9vTWsTZFduj9_EAc_MkJw2DQKrJAKVwqm_k130_assertion wasDerivedFrom befree-20140225 NP574584.RA1DgwVwTj9vTWsTZFduj9_EAc_MkJw2DQKrJAKVwqm_k130_provenance.
- NP574584.RA1DgwVwTj9vTWsTZFduj9_EAc_MkJw2DQKrJAKVwqm_k130_assertion wasGeneratedBy ECO_0000203 NP574584.RA1DgwVwTj9vTWsTZFduj9_EAc_MkJw2DQKrJAKVwqm_k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP574584.RA1DgwVwTj9vTWsTZFduj9_EAc_MkJw2DQKrJAKVwqm_k130_provenance.