Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP211916.RA5lR2yL9BnMUGxvQDv78vl3h9lcCm6NayyZSbaw-hRno130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP211916.RA5lR2yL9BnMUGxvQDv78vl3h9lcCm6NayyZSbaw-hRno130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP211916.RA5lR2yL9BnMUGxvQDv78vl3h9lcCm6NayyZSbaw-hRno130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP211916.RA5lR2yL9BnMUGxvQDv78vl3h9lcCm6NayyZSbaw-hRno130_provenance.
- NP211916.RA5lR2yL9BnMUGxvQDv78vl3h9lcCm6NayyZSbaw-hRno130_assertion description "[The imprinted Snurf-Snrpn chromosomal domain contains two large arrays of tandemly repeated, paternally expressed box C/D small-nucleolar RNA (snoRNA) genes: the SNORD115 (H/MBII-52) and SNORD116 (H/MBII-85) gene clusters believed to play key roles in the fine-tuning of serotonin receptor (5-HT2C) pre-mRNA processing and in the etiology of the Prader-Willi Syndrome (PWS), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP211916.RA5lR2yL9BnMUGxvQDv78vl3h9lcCm6NayyZSbaw-hRno130_provenance.
- NP211916.RA5lR2yL9BnMUGxvQDv78vl3h9lcCm6NayyZSbaw-hRno130_assertion evidence source_evidence_literature NP211916.RA5lR2yL9BnMUGxvQDv78vl3h9lcCm6NayyZSbaw-hRno130_provenance.
- NP211916.RA5lR2yL9BnMUGxvQDv78vl3h9lcCm6NayyZSbaw-hRno130_assertion SIO_000772 22495932 NP211916.RA5lR2yL9BnMUGxvQDv78vl3h9lcCm6NayyZSbaw-hRno130_provenance.
- NP211916.RA5lR2yL9BnMUGxvQDv78vl3h9lcCm6NayyZSbaw-hRno130_assertion wasDerivedFrom befree-20140225 NP211916.RA5lR2yL9BnMUGxvQDv78vl3h9lcCm6NayyZSbaw-hRno130_provenance.
- NP211916.RA5lR2yL9BnMUGxvQDv78vl3h9lcCm6NayyZSbaw-hRno130_assertion wasGeneratedBy ECO_0000203 NP211916.RA5lR2yL9BnMUGxvQDv78vl3h9lcCm6NayyZSbaw-hRno130_provenance.
- befree-20140225 importedOn "2014-02-25" NP211916.RA5lR2yL9BnMUGxvQDv78vl3h9lcCm6NayyZSbaw-hRno130_provenance.