@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:NP256731.RAls2ZPG34vcePfVZhzRzua7ETi8-Vuav7E0okt1HJl2k130_head { this: np:hasAssertion dgn-np:NP256731.RAls2ZPG34vcePfVZhzRzua7ETi8-Vuav7E0okt1HJl2k130_assertion; np:hasProvenance dgn-np:NP256731.RAls2ZPG34vcePfVZhzRzua7ETi8-Vuav7E0okt1HJl2k130_provenance; np:hasPublicationInfo dgn-np:NP256731.RAls2ZPG34vcePfVZhzRzua7ETi8-Vuav7E0okt1HJl2k130_publicationInfo; a np:Nanopublication . dgn-np:NP256731.RAls2ZPG34vcePfVZhzRzua7ETi8-Vuav7E0okt1HJl2k130_assertion a np:Assertion . dgn-np:NP256731.RAls2ZPG34vcePfVZhzRzua7ETi8-Vuav7E0okt1HJl2k130_provenance a np:Provenance . dgn-np:NP256731.RAls2ZPG34vcePfVZhzRzua7ETi8-Vuav7E0okt1HJl2k130_publicationInfo a np:PublicationInfo . } dgn-np:NP256731.RAls2ZPG34vcePfVZhzRzua7ETi8-Vuav7E0okt1HJl2k130_assertion { miriam-gene:4221 a ncit:C16612 . lld:C0027662 a ncit:C7057 . dgn-gda:DGNbc3e4c9fe65b031465db78bcde617a04 sio:SIO_000628 miriam-gene:4221, lld:C0027662; a sio:SIO_001121 . } dgn-np:NP256731.RAls2ZPG34vcePfVZhzRzua7ETi8-Vuav7E0okt1HJl2k130_provenance { dgn-np:NP256731.RAls2ZPG34vcePfVZhzRzua7ETi8-Vuav7E0okt1HJl2k130_assertion dcterms:description "[FHPT consists of a variety of diseases such as multiple endocrine neoplasia type1 (MEN 1) and type2 (MEN 2), familial isolated hyperparathyroidism (FIHPT) with single adenoma and with multiple adenomas (or hyperplasia), and FHPT with jaw-tumor (FHPT-JT).]. 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:10395244; 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:NP256731.RAls2ZPG34vcePfVZhzRzua7ETi8-Vuav7E0okt1HJl2k130_publicationInfo { this: dcterms:created "2016-05-13T12:43:42+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" . }