@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP690268.RAK0KLPe8HUly0TU2wdVzU_4_H5AHX5neKo6wdj1hGI9Q130_head { this: np:hasAssertion dgn-np:NP690268.RAK0KLPe8HUly0TU2wdVzU_4_H5AHX5neKo6wdj1hGI9Q130_assertion; np:hasProvenance dgn-np:NP690268.RAK0KLPe8HUly0TU2wdVzU_4_H5AHX5neKo6wdj1hGI9Q130_provenance; np:hasPublicationInfo dgn-np:NP690268.RAK0KLPe8HUly0TU2wdVzU_4_H5AHX5neKo6wdj1hGI9Q130_publicationInfo; a np:Nanopublication . dgn-np:NP690268.RAK0KLPe8HUly0TU2wdVzU_4_H5AHX5neKo6wdj1hGI9Q130_assertion a np:Assertion . dgn-np:NP690268.RAK0KLPe8HUly0TU2wdVzU_4_H5AHX5neKo6wdj1hGI9Q130_provenance a np:Provenance . dgn-np:NP690268.RAK0KLPe8HUly0TU2wdVzU_4_H5AHX5neKo6wdj1hGI9Q130_publicationInfo a np:PublicationInfo . } dgn-np:NP690268.RAK0KLPe8HUly0TU2wdVzU_4_H5AHX5neKo6wdj1hGI9Q130_assertion { miriam-gene:3925 a ncit:C16612 . lld:C0027868 a ncit:C7057 . dgn-gda:DGN6f86cc1d32fc22613eb52405cce52cdc sio:SIO_000628 miriam-gene:3925, lld:C0027868; a sio:SIO_001121 . } dgn-np:NP690268.RAK0KLPe8HUly0TU2wdVzU_4_H5AHX5neKo6wdj1hGI9Q130_provenance { dgn-np:NP690268.RAK0KLPe8HUly0TU2wdVzU_4_H5AHX5neKo6wdj1hGI9Q130_assertion dcterms:description "[Over the last 10 years, research into the function of Cajal bodies has been greatly stimulated by the discovery that SMN, the protein deficient in the inherited neuromuscular disease, spinal muscular atrophy, is a Cajal body component and has an essential role in the assembly of spliceosomal U snRNPs in the cytoplasm and their delivery to the Cajal body in the nucleus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:18755223; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP690268.RAK0KLPe8HUly0TU2wdVzU_4_H5AHX5neKo6wdj1hGI9Q130_publicationInfo { this: dcterms:created "2016-05-13T12:46:58+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }