@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:NP1402161.RAOzGnDFWAYyRNiNBaw9arJOwK8iLgSa8x8LvHl0FeFaU130_head { this: np:hasAssertion dgn-np:NP1402161.RAOzGnDFWAYyRNiNBaw9arJOwK8iLgSa8x8LvHl0FeFaU130_assertion; np:hasProvenance dgn-np:NP1402161.RAOzGnDFWAYyRNiNBaw9arJOwK8iLgSa8x8LvHl0FeFaU130_provenance; np:hasPublicationInfo dgn-np:NP1402161.RAOzGnDFWAYyRNiNBaw9arJOwK8iLgSa8x8LvHl0FeFaU130_publicationInfo; a np:Nanopublication . dgn-np:NP1402161.RAOzGnDFWAYyRNiNBaw9arJOwK8iLgSa8x8LvHl0FeFaU130_assertion a np:Assertion . dgn-np:NP1402161.RAOzGnDFWAYyRNiNBaw9arJOwK8iLgSa8x8LvHl0FeFaU130_provenance a np:Provenance . dgn-np:NP1402161.RAOzGnDFWAYyRNiNBaw9arJOwK8iLgSa8x8LvHl0FeFaU130_publicationInfo a np:PublicationInfo . } dgn-np:NP1402161.RAOzGnDFWAYyRNiNBaw9arJOwK8iLgSa8x8LvHl0FeFaU130_assertion { miriam-gene:138428 a ncit:C16612 . lld:C0221002 a ncit:C7057 . dgn-gda:DGN25e740754ba7fa88008038e90fa31e92 sio:SIO_000628 miriam-gene:138428, lld:C0221002; a sio:SIO_001121 . } dgn-np:NP1402161.RAOzGnDFWAYyRNiNBaw9arJOwK8iLgSa8x8LvHl0FeFaU130_provenance { dgn-np:NP1402161.RAOzGnDFWAYyRNiNBaw9arJOwK8iLgSa8x8LvHl0FeFaU130_assertion dcterms:description "[However, the demonstration of LOH at 11q13 and MEN1 gene mutations in small parathyroid adenomas of patients with slight hypercalcemia and normal serum PTH levels suggest that altered MEN1 gene function may also be important for the development of mild sporadic pHPT.]. 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:9709976; 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:NP1402161.RAOzGnDFWAYyRNiNBaw9arJOwK8iLgSa8x8LvHl0FeFaU130_publicationInfo { this: dcterms:created "2016-05-13T12:52:21+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" . }