Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP362681.RABrUT1EPdGwNzHPrDTnx49aSWEevaeCCfyNwVhJ3K8as130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP362681.RABrUT1EPdGwNzHPrDTnx49aSWEevaeCCfyNwVhJ3K8as130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP362681.RABrUT1EPdGwNzHPrDTnx49aSWEevaeCCfyNwVhJ3K8as130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP362681.RABrUT1EPdGwNzHPrDTnx49aSWEevaeCCfyNwVhJ3K8as130_provenance.
- befree-20150227 importedOn "2015-02-27" NP362681.RABrUT1EPdGwNzHPrDTnx49aSWEevaeCCfyNwVhJ3K8as130_provenance.
- NP362681.RABrUT1EPdGwNzHPrDTnx49aSWEevaeCCfyNwVhJ3K8as130_assertion wasGeneratedBy ECO_0000203 NP362681.RABrUT1EPdGwNzHPrDTnx49aSWEevaeCCfyNwVhJ3K8as130_provenance.
- NP362681.RABrUT1EPdGwNzHPrDTnx49aSWEevaeCCfyNwVhJ3K8as130_assertion wasDerivedFrom befree-20150227 NP362681.RABrUT1EPdGwNzHPrDTnx49aSWEevaeCCfyNwVhJ3K8as130_provenance.
- NP362681.RABrUT1EPdGwNzHPrDTnx49aSWEevaeCCfyNwVhJ3K8as130_assertion SIO_000772 18405873 NP362681.RABrUT1EPdGwNzHPrDTnx49aSWEevaeCCfyNwVhJ3K8as130_provenance.
- NP362681.RABrUT1EPdGwNzHPrDTnx49aSWEevaeCCfyNwVhJ3K8as130_assertion evidence source_evidence_literature NP362681.RABrUT1EPdGwNzHPrDTnx49aSWEevaeCCfyNwVhJ3K8as130_provenance.
- NP362681.RABrUT1EPdGwNzHPrDTnx49aSWEevaeCCfyNwVhJ3K8as130_assertion description "[We have identified and characterized two unrelated patients with prenatal onset of microcephaly, intrauterine growth retardation, feeding problems, developmental delay, and febrile seizures/epilepsy who both carry a de novo balanced translocation that truncates the DYRK1A gene at chromosome 21q22.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP362681.RABrUT1EPdGwNzHPrDTnx49aSWEevaeCCfyNwVhJ3K8as130_provenance.