Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_provenance.
- NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_assertion wasGeneratedBy ECO_0000203 NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_provenance.
- NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_assertion wasDerivedFrom befree-20150227 NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_provenance.
- NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_assertion SIO_000772 9615224 NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_provenance.
- NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_assertion evidence source_evidence_literature NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_provenance.
- NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_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." NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_provenance.