@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:NP939936.RAdHj7dlor7uwSKvvmPjc_MHnf9IdSaq0V0m7esEI-xrY130_head { this: np:hasAssertion dgn-np:NP939936.RAdHj7dlor7uwSKvvmPjc_MHnf9IdSaq0V0m7esEI-xrY130_assertion; np:hasProvenance dgn-np:NP939936.RAdHj7dlor7uwSKvvmPjc_MHnf9IdSaq0V0m7esEI-xrY130_provenance; np:hasPublicationInfo dgn-np:NP939936.RAdHj7dlor7uwSKvvmPjc_MHnf9IdSaq0V0m7esEI-xrY130_publicationInfo; a np:Nanopublication . dgn-np:NP939936.RAdHj7dlor7uwSKvvmPjc_MHnf9IdSaq0V0m7esEI-xrY130_assertion a np:Assertion . dgn-np:NP939936.RAdHj7dlor7uwSKvvmPjc_MHnf9IdSaq0V0m7esEI-xrY130_provenance a np:Provenance . dgn-np:NP939936.RAdHj7dlor7uwSKvvmPjc_MHnf9IdSaq0V0m7esEI-xrY130_publicationInfo a np:PublicationInfo . } dgn-np:NP939936.RAdHj7dlor7uwSKvvmPjc_MHnf9IdSaq0V0m7esEI-xrY130_assertion { miriam-gene:1759 a ncit:C16612 . lld:C0007959 a ncit:C7057 . dgn-gda:DGNfc8baed2507f7307b18d61df15ff44e7 sio:SIO_000628 miriam-gene:1759, lld:C0007959; a sio:SIO_001121 . } dgn-np:NP939936.RAdHj7dlor7uwSKvvmPjc_MHnf9IdSaq0V0m7esEI-xrY130_provenance { dgn-np:NP939936.RAdHj7dlor7uwSKvvmPjc_MHnf9IdSaq0V0m7esEI-xrY130_assertion dcterms:description "[Furthermore, CNM mutants were seen in association with enlarged clathrin stained structures whereas the CMT mutant constructs were associated with clathrin structures that appeared clustered, similar to the structures observed in Dnm1 and Dnm2 double knock-out cells.]. 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:22096584; 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:NP939936.RAdHj7dlor7uwSKvvmPjc_MHnf9IdSaq0V0m7esEI-xrY130_publicationInfo { this: dcterms:created "2016-05-13T12:48:51+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" . }