Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP859434.RAkYmeexCmnTBh6Iw91x3NNVnd0lRZT_IlzHyAx_IIX4c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP859434.RAkYmeexCmnTBh6Iw91x3NNVnd0lRZT_IlzHyAx_IIX4c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP859434.RAkYmeexCmnTBh6Iw91x3NNVnd0lRZT_IlzHyAx_IIX4c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP859434.RAkYmeexCmnTBh6Iw91x3NNVnd0lRZT_IlzHyAx_IIX4c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP859434.RAkYmeexCmnTBh6Iw91x3NNVnd0lRZT_IlzHyAx_IIX4c130_provenance.
- NP859434.RAkYmeexCmnTBh6Iw91x3NNVnd0lRZT_IlzHyAx_IIX4c130_assertion wasGeneratedBy ECO_0000203 NP859434.RAkYmeexCmnTBh6Iw91x3NNVnd0lRZT_IlzHyAx_IIX4c130_provenance.
- NP859434.RAkYmeexCmnTBh6Iw91x3NNVnd0lRZT_IlzHyAx_IIX4c130_assertion wasDerivedFrom befree-20150227 NP859434.RAkYmeexCmnTBh6Iw91x3NNVnd0lRZT_IlzHyAx_IIX4c130_provenance.
- NP859434.RAkYmeexCmnTBh6Iw91x3NNVnd0lRZT_IlzHyAx_IIX4c130_assertion SIO_000772 9615224 NP859434.RAkYmeexCmnTBh6Iw91x3NNVnd0lRZT_IlzHyAx_IIX4c130_provenance.
- NP859434.RAkYmeexCmnTBh6Iw91x3NNVnd0lRZT_IlzHyAx_IIX4c130_assertion evidence source_evidence_literature NP859434.RAkYmeexCmnTBh6Iw91x3NNVnd0lRZT_IlzHyAx_IIX4c130_provenance.
- NP859434.RAkYmeexCmnTBh6Iw91x3NNVnd0lRZT_IlzHyAx_IIX4c130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP859434.RAkYmeexCmnTBh6Iw91x3NNVnd0lRZT_IlzHyAx_IIX4c130_provenance.