@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:NP662526.RALc5SJdzTKJOoE9-5gCzk78CF_cckdApiU3By4wj4hp8130_head { this: np:hasAssertion dgn-np:NP662526.RALc5SJdzTKJOoE9-5gCzk78CF_cckdApiU3By4wj4hp8130_assertion; np:hasProvenance dgn-np:NP662526.RALc5SJdzTKJOoE9-5gCzk78CF_cckdApiU3By4wj4hp8130_provenance; np:hasPublicationInfo dgn-np:NP662526.RALc5SJdzTKJOoE9-5gCzk78CF_cckdApiU3By4wj4hp8130_publicationInfo; a np:Nanopublication . dgn-np:NP662526.RALc5SJdzTKJOoE9-5gCzk78CF_cckdApiU3By4wj4hp8130_assertion a np:Assertion . dgn-np:NP662526.RALc5SJdzTKJOoE9-5gCzk78CF_cckdApiU3By4wj4hp8130_provenance a np:Provenance . dgn-np:NP662526.RALc5SJdzTKJOoE9-5gCzk78CF_cckdApiU3By4wj4hp8130_publicationInfo a np:PublicationInfo . } dgn-np:NP662526.RALc5SJdzTKJOoE9-5gCzk78CF_cckdApiU3By4wj4hp8130_assertion { miriam-gene:5837 a ncit:C16612 . lld:C0021670 a ncit:C7057 . dgn-gda:DGNcdb24179d08dacc3c05951d942bb0b64 sio:SIO_000628 miriam-gene:5837, lld:C0021670; a sio:SIO_001121 . } dgn-np:NP662526.RALc5SJdzTKJOoE9-5gCzk78CF_cckdApiU3By4wj4hp8130_provenance { dgn-np:NP662526.RALc5SJdzTKJOoE9-5gCzk78CF_cckdApiU3By4wj4hp8130_assertion dcterms:description "[We have therefore undertaken studies to search for such mutations in six MEN type 1 tumors (four parathyroid tumors, one insulinoma, and one lipoma) that did not have LOH at 11q13 as assessed using the flanking markers D11S480, D11S1883 and PYGM centromerically and D11S449 and D11S913 telomerically.]. 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:11549677; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP662526.RALc5SJdzTKJOoE9-5gCzk78CF_cckdApiU3By4wj4hp8130_publicationInfo { this: dcterms:created "2015-08-25T14:44:18+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }