@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:NP497084.RA7q8KkcW7PwmJfwxRgp00cZNMp1viwlU0kl1hmts0N98130_head { this: np:hasAssertion dgn-np:NP497084.RA7q8KkcW7PwmJfwxRgp00cZNMp1viwlU0kl1hmts0N98130_assertion; np:hasProvenance dgn-np:NP497084.RA7q8KkcW7PwmJfwxRgp00cZNMp1viwlU0kl1hmts0N98130_provenance; np:hasPublicationInfo dgn-np:NP497084.RA7q8KkcW7PwmJfwxRgp00cZNMp1viwlU0kl1hmts0N98130_publicationInfo; a np:Nanopublication . dgn-np:NP497084.RA7q8KkcW7PwmJfwxRgp00cZNMp1viwlU0kl1hmts0N98130_assertion a np:Assertion . dgn-np:NP497084.RA7q8KkcW7PwmJfwxRgp00cZNMp1viwlU0kl1hmts0N98130_provenance a np:Provenance . dgn-np:NP497084.RA7q8KkcW7PwmJfwxRgp00cZNMp1viwlU0kl1hmts0N98130_publicationInfo a np:PublicationInfo . } dgn-np:NP497084.RA7q8KkcW7PwmJfwxRgp00cZNMp1viwlU0kl1hmts0N98130_assertion { miriam-gene:5573 a ncit:C16612 . lld:C0406810 a ncit:C7057 . dgn-gda:DGNfaeccbff4ee831f0a629bcc1ff6d7d67 sio:SIO_000628 miriam-gene:5573, lld:C0406810; a sio:SIO_001121 . } dgn-np:NP497084.RA7q8KkcW7PwmJfwxRgp00cZNMp1viwlU0kl1hmts0N98130_provenance { dgn-np:NP497084.RA7q8KkcW7PwmJfwxRgp00cZNMp1viwlU0kl1hmts0N98130_assertion dcterms:description "[Recently, mutations of the gene encoding the PKA type 1 A regulatory subunit (R1 A), PRKAR1A, associated with loss of heterozygosity (LOH) at PRKAR1A locus, have been demonstrated in primary pigmented nodular adrenocortical disease (PPNAD), either isolated or associated with Carney complex.]. 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:15926108; 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:NP497084.RA7q8KkcW7PwmJfwxRgp00cZNMp1viwlU0kl1hmts0N98130_publicationInfo { this: dcterms:created "2016-05-13T12:45:30+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" . }