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- source_evidence_literature type ECO_0000212 NP665340.RAIy-rT2RR8Yl3BQC05UY_3wdnrE2LZFrcxMhi1ycI508130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP665340.RAIy-rT2RR8Yl3BQC05UY_3wdnrE2LZFrcxMhi1ycI508130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP665340.RAIy-rT2RR8Yl3BQC05UY_3wdnrE2LZFrcxMhi1ycI508130_provenance.
- befree-2016 importedOn "2016-02-19" NP665340.RAIy-rT2RR8Yl3BQC05UY_3wdnrE2LZFrcxMhi1ycI508130_provenance.
- NP665340.RAIy-rT2RR8Yl3BQC05UY_3wdnrE2LZFrcxMhi1ycI508130_assertion wasGeneratedBy ECO_0000203 NP665340.RAIy-rT2RR8Yl3BQC05UY_3wdnrE2LZFrcxMhi1ycI508130_provenance.
- NP665340.RAIy-rT2RR8Yl3BQC05UY_3wdnrE2LZFrcxMhi1ycI508130_assertion wasDerivedFrom befree-2016 NP665340.RAIy-rT2RR8Yl3BQC05UY_3wdnrE2LZFrcxMhi1ycI508130_provenance.
- NP665340.RAIy-rT2RR8Yl3BQC05UY_3wdnrE2LZFrcxMhi1ycI508130_assertion SIO_000772 18405873 NP665340.RAIy-rT2RR8Yl3BQC05UY_3wdnrE2LZFrcxMhi1ycI508130_provenance.
- NP665340.RAIy-rT2RR8Yl3BQC05UY_3wdnrE2LZFrcxMhi1ycI508130_assertion evidence source_evidence_literature NP665340.RAIy-rT2RR8Yl3BQC05UY_3wdnrE2LZFrcxMhi1ycI508130_provenance.
- NP665340.RAIy-rT2RR8Yl3BQC05UY_3wdnrE2LZFrcxMhi1ycI508130_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." NP665340.RAIy-rT2RR8Yl3BQC05UY_3wdnrE2LZFrcxMhi1ycI508130_provenance.