@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:NP1353421.RAzgiI7ORVcLmkQ5FdkkZMxDJbO3fVQrWmveGoznqZ-nY130_head { this: np:hasAssertion dgn-np:NP1353421.RAzgiI7ORVcLmkQ5FdkkZMxDJbO3fVQrWmveGoznqZ-nY130_assertion; np:hasProvenance dgn-np:NP1353421.RAzgiI7ORVcLmkQ5FdkkZMxDJbO3fVQrWmveGoznqZ-nY130_provenance; np:hasPublicationInfo dgn-np:NP1353421.RAzgiI7ORVcLmkQ5FdkkZMxDJbO3fVQrWmveGoznqZ-nY130_publicationInfo; a np:Nanopublication . dgn-np:NP1353421.RAzgiI7ORVcLmkQ5FdkkZMxDJbO3fVQrWmveGoznqZ-nY130_assertion a np:Assertion . dgn-np:NP1353421.RAzgiI7ORVcLmkQ5FdkkZMxDJbO3fVQrWmveGoznqZ-nY130_provenance a np:Provenance . dgn-np:NP1353421.RAzgiI7ORVcLmkQ5FdkkZMxDJbO3fVQrWmveGoznqZ-nY130_publicationInfo a np:PublicationInfo . } dgn-np:NP1353421.RAzgiI7ORVcLmkQ5FdkkZMxDJbO3fVQrWmveGoznqZ-nY130_assertion { miriam-gene:2778 a ncit:C16612 . lld:C0259779 a ncit:C7057 . dgn-gda:DGN5950b2f81cc48f81bca6a42cb7a3ec5d sio:SIO_000628 miriam-gene:2778, lld:C0259779; a sio:SIO_001121 . } dgn-np:NP1353421.RAzgiI7ORVcLmkQ5FdkkZMxDJbO3fVQrWmveGoznqZ-nY130_provenance { dgn-np:NP1353421.RAzgiI7ORVcLmkQ5FdkkZMxDJbO3fVQrWmveGoznqZ-nY130_assertion dcterms:description "[Acquisition of a similar activating mutation in GNAS1 later in life presumably accounts for the restricted distribution of the gsp oncogene, and is associated with the development of isolated lesions (for example, fibrous dysplasia, pituitary or thyroid tumors) without other manifestations of MAS.]. 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:8699958; 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:NP1353421.RAzgiI7ORVcLmkQ5FdkkZMxDJbO3fVQrWmveGoznqZ-nY130_publicationInfo { this: dcterms:created "2016-05-13T12:51:59+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" . }