@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:NP390993.RAOiE_4nCnt6kOaUoyn-d7Qai2mthjIwy3cxANTLsHYgM130_head { this: np:hasAssertion dgn-np:NP390993.RAOiE_4nCnt6kOaUoyn-d7Qai2mthjIwy3cxANTLsHYgM130_assertion; np:hasProvenance dgn-np:NP390993.RAOiE_4nCnt6kOaUoyn-d7Qai2mthjIwy3cxANTLsHYgM130_provenance; np:hasPublicationInfo dgn-np:NP390993.RAOiE_4nCnt6kOaUoyn-d7Qai2mthjIwy3cxANTLsHYgM130_publicationInfo; a np:Nanopublication . dgn-np:NP390993.RAOiE_4nCnt6kOaUoyn-d7Qai2mthjIwy3cxANTLsHYgM130_assertion a np:Assertion . dgn-np:NP390993.RAOiE_4nCnt6kOaUoyn-d7Qai2mthjIwy3cxANTLsHYgM130_provenance a np:Provenance . dgn-np:NP390993.RAOiE_4nCnt6kOaUoyn-d7Qai2mthjIwy3cxANTLsHYgM130_publicationInfo a np:PublicationInfo . } dgn-np:NP390993.RAOiE_4nCnt6kOaUoyn-d7Qai2mthjIwy3cxANTLsHYgM130_assertion { miriam-gene:6757 a ncit:C16612 . lld:C0039101 a ncit:C7057 . dgn-gda:DGN8a853eb2f2b658c7e6dd482c99e19d87 sio:SIO_000628 miriam-gene:6757, lld:C0039101; a sio:SIO_001121 . } dgn-np:NP390993.RAOiE_4nCnt6kOaUoyn-d7Qai2mthjIwy3cxANTLsHYgM130_provenance { dgn-np:NP390993.RAOiE_4nCnt6kOaUoyn-d7Qai2mthjIwy3cxANTLsHYgM130_assertion dcterms:description "[Because SS18/SSX fusions do not seem to occur in other tumor types, and because synovial sarcomas may sometimes be difficult to distinguish from other spindle cell tumors, molecular genetic analysis has become established as an important diagnostic tool.]. 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:12696068; 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:NP390993.RAOiE_4nCnt6kOaUoyn-d7Qai2mthjIwy3cxANTLsHYgM130_publicationInfo { this: dcterms:created "2016-05-13T12:44:42+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" . }