Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP502677.RA17vwFxppDVohuRp4IgQIOClD9ivoYvZ8aqAj1vh4nrs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP502677.RA17vwFxppDVohuRp4IgQIOClD9ivoYvZ8aqAj1vh4nrs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP502677.RA17vwFxppDVohuRp4IgQIOClD9ivoYvZ8aqAj1vh4nrs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP502677.RA17vwFxppDVohuRp4IgQIOClD9ivoYvZ8aqAj1vh4nrs130_provenance.
- befree-2016 importedOn "2016-02-19" NP502677.RA17vwFxppDVohuRp4IgQIOClD9ivoYvZ8aqAj1vh4nrs130_provenance.
- NP502677.RA17vwFxppDVohuRp4IgQIOClD9ivoYvZ8aqAj1vh4nrs130_assertion wasGeneratedBy ECO_0000203 NP502677.RA17vwFxppDVohuRp4IgQIOClD9ivoYvZ8aqAj1vh4nrs130_provenance.
- NP502677.RA17vwFxppDVohuRp4IgQIOClD9ivoYvZ8aqAj1vh4nrs130_assertion wasDerivedFrom befree-2016 NP502677.RA17vwFxppDVohuRp4IgQIOClD9ivoYvZ8aqAj1vh4nrs130_provenance.
- NP502677.RA17vwFxppDVohuRp4IgQIOClD9ivoYvZ8aqAj1vh4nrs130_assertion SIO_000772 16000562 NP502677.RA17vwFxppDVohuRp4IgQIOClD9ivoYvZ8aqAj1vh4nrs130_provenance.
- NP502677.RA17vwFxppDVohuRp4IgQIOClD9ivoYvZ8aqAj1vh4nrs130_assertion evidence source_evidence_literature NP502677.RA17vwFxppDVohuRp4IgQIOClD9ivoYvZ8aqAj1vh4nrs130_provenance.
- NP502677.RA17vwFxppDVohuRp4IgQIOClD9ivoYvZ8aqAj1vh4nrs130_assertion description "[We report here the first identification of a homozygous mutation in MSH6 in a family with childhood-onset brain tumor, lymphoma, colorectal cancer, and neurofibromatosis type 1 phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP502677.RA17vwFxppDVohuRp4IgQIOClD9ivoYvZ8aqAj1vh4nrs130_provenance.