Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP908147.RAfkhu35DOMrEVeaaxgf2UNvGK3REZcXuzBeLvyv2u-Bc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP908147.RAfkhu35DOMrEVeaaxgf2UNvGK3REZcXuzBeLvyv2u-Bc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP908147.RAfkhu35DOMrEVeaaxgf2UNvGK3REZcXuzBeLvyv2u-Bc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP908147.RAfkhu35DOMrEVeaaxgf2UNvGK3REZcXuzBeLvyv2u-Bc130_provenance.
- NP908147.RAfkhu35DOMrEVeaaxgf2UNvGK3REZcXuzBeLvyv2u-Bc130_assertion description "[The phenotype of paternal UPD6 results from biallelic expression of the maternally imprinted, paternally expressed ZAC and HYMAI genes, and includes transient neonatal diabetes mellitus (TNDM), intra-uterine growth restriction (IUGR), macroglossia, and minor anomalies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP908147.RAfkhu35DOMrEVeaaxgf2UNvGK3REZcXuzBeLvyv2u-Bc130_provenance.
- NP908147.RAfkhu35DOMrEVeaaxgf2UNvGK3REZcXuzBeLvyv2u-Bc130_assertion evidence source_evidence_literature NP908147.RAfkhu35DOMrEVeaaxgf2UNvGK3REZcXuzBeLvyv2u-Bc130_provenance.
- NP908147.RAfkhu35DOMrEVeaaxgf2UNvGK3REZcXuzBeLvyv2u-Bc130_assertion SIO_000772 21739591 NP908147.RAfkhu35DOMrEVeaaxgf2UNvGK3REZcXuzBeLvyv2u-Bc130_provenance.
- NP908147.RAfkhu35DOMrEVeaaxgf2UNvGK3REZcXuzBeLvyv2u-Bc130_assertion wasDerivedFrom befree-2016 NP908147.RAfkhu35DOMrEVeaaxgf2UNvGK3REZcXuzBeLvyv2u-Bc130_provenance.
- NP908147.RAfkhu35DOMrEVeaaxgf2UNvGK3REZcXuzBeLvyv2u-Bc130_assertion wasGeneratedBy ECO_0000203 NP908147.RAfkhu35DOMrEVeaaxgf2UNvGK3REZcXuzBeLvyv2u-Bc130_provenance.
- befree-2016 importedOn "2016-02-19" NP908147.RAfkhu35DOMrEVeaaxgf2UNvGK3REZcXuzBeLvyv2u-Bc130_provenance.