Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP569911.RAzLtoL1l9GnWwgfHu2ov4XEBIQorwlVerithmwC_58SY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP569911.RAzLtoL1l9GnWwgfHu2ov4XEBIQorwlVerithmwC_58SY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569911.RAzLtoL1l9GnWwgfHu2ov4XEBIQorwlVerithmwC_58SY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569911.RAzLtoL1l9GnWwgfHu2ov4XEBIQorwlVerithmwC_58SY130_provenance.
- NP569911.RAzLtoL1l9GnWwgfHu2ov4XEBIQorwlVerithmwC_58SY130_assertion description "[Four genes (NIPA1, NIPA2, CYFIP1, and GCP5) have been identified in the chromosomal region between breakpoints 1 and 2 and are implicated in compulsive behavior and lower intellectual ability observed in individuals with Prader-Willi syndrome with TI versus TII deletions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569911.RAzLtoL1l9GnWwgfHu2ov4XEBIQorwlVerithmwC_58SY130_provenance.
- NP569911.RAzLtoL1l9GnWwgfHu2ov4XEBIQorwlVerithmwC_58SY130_assertion evidence source_evidence_literature NP569911.RAzLtoL1l9GnWwgfHu2ov4XEBIQorwlVerithmwC_58SY130_provenance.
- NP569911.RAzLtoL1l9GnWwgfHu2ov4XEBIQorwlVerithmwC_58SY130_assertion SIO_000772 16982806 NP569911.RAzLtoL1l9GnWwgfHu2ov4XEBIQorwlVerithmwC_58SY130_provenance.
- NP569911.RAzLtoL1l9GnWwgfHu2ov4XEBIQorwlVerithmwC_58SY130_assertion wasDerivedFrom befree-2016 NP569911.RAzLtoL1l9GnWwgfHu2ov4XEBIQorwlVerithmwC_58SY130_provenance.
- NP569911.RAzLtoL1l9GnWwgfHu2ov4XEBIQorwlVerithmwC_58SY130_assertion wasGeneratedBy ECO_0000203 NP569911.RAzLtoL1l9GnWwgfHu2ov4XEBIQorwlVerithmwC_58SY130_provenance.
- befree-2016 importedOn "2016-02-19" NP569911.RAzLtoL1l9GnWwgfHu2ov4XEBIQorwlVerithmwC_58SY130_provenance.