@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:NP933654.RArMIeBXWWpX-R2zsat8J_HdlzfC5gKyNZ4aFi11lfWa4130_head { this: np:hasAssertion dgn-np:NP933654.RArMIeBXWWpX-R2zsat8J_HdlzfC5gKyNZ4aFi11lfWa4130_assertion; np:hasProvenance dgn-np:NP933654.RArMIeBXWWpX-R2zsat8J_HdlzfC5gKyNZ4aFi11lfWa4130_provenance; np:hasPublicationInfo dgn-np:NP933654.RArMIeBXWWpX-R2zsat8J_HdlzfC5gKyNZ4aFi11lfWa4130_publicationInfo; a np:Nanopublication . dgn-np:NP933654.RArMIeBXWWpX-R2zsat8J_HdlzfC5gKyNZ4aFi11lfWa4130_assertion a np:Assertion . dgn-np:NP933654.RArMIeBXWWpX-R2zsat8J_HdlzfC5gKyNZ4aFi11lfWa4130_provenance a np:Provenance . dgn-np:NP933654.RArMIeBXWWpX-R2zsat8J_HdlzfC5gKyNZ4aFi11lfWa4130_publicationInfo a np:PublicationInfo . } dgn-np:NP933654.RArMIeBXWWpX-R2zsat8J_HdlzfC5gKyNZ4aFi11lfWa4130_assertion { miriam-gene:6469 a ncit:C16612 . lld:C1511789 a ncit:C7057 . dgn-gda:DGNc6dcbb4628f58c255cb2af9c84b437dd sio:SIO_000628 miriam-gene:6469, lld:C1511789; a sio:SIO_001121 . } dgn-np:NP933654.RArMIeBXWWpX-R2zsat8J_HdlzfC5gKyNZ4aFi11lfWa4130_provenance { dgn-np:NP933654.RArMIeBXWWpX-R2zsat8J_HdlzfC5gKyNZ4aFi11lfWa4130_assertion dcterms:description "[Activation of the sonic hedgehog pathway with frequent mutations of the PTCH and SUFU genes, loss of 9q, and positivity for GLI1 and SFRP1 is more frequent in children less than 3 years old and in adults, commonly associated with desmoplastic histology.]. 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:22027544; 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:NP933654.RArMIeBXWWpX-R2zsat8J_HdlzfC5gKyNZ4aFi11lfWa4130_publicationInfo { this: dcterms:created "2016-05-13T12:48:48+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" . }