@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:NP243390.RAiSQg9b-iTAb2J2EamQy-lAmOaco8t11JLu-nh3Dj9MA130_head { this: np:hasAssertion dgn-np:NP243390.RAiSQg9b-iTAb2J2EamQy-lAmOaco8t11JLu-nh3Dj9MA130_assertion; np:hasProvenance dgn-np:NP243390.RAiSQg9b-iTAb2J2EamQy-lAmOaco8t11JLu-nh3Dj9MA130_provenance; np:hasPublicationInfo dgn-np:NP243390.RAiSQg9b-iTAb2J2EamQy-lAmOaco8t11JLu-nh3Dj9MA130_publicationInfo; a np:Nanopublication . dgn-np:NP243390.RAiSQg9b-iTAb2J2EamQy-lAmOaco8t11JLu-nh3Dj9MA130_assertion a np:Assertion . dgn-np:NP243390.RAiSQg9b-iTAb2J2EamQy-lAmOaco8t11JLu-nh3Dj9MA130_provenance a np:Provenance . dgn-np:NP243390.RAiSQg9b-iTAb2J2EamQy-lAmOaco8t11JLu-nh3Dj9MA130_publicationInfo a np:PublicationInfo . } dgn-np:NP243390.RAiSQg9b-iTAb2J2EamQy-lAmOaco8t11JLu-nh3Dj9MA130_assertion { miriam-gene:335 a ncit:C16612 . lld:C0268380 a ncit:C7057 . dgn-gda:DGNb7070743963692c5ff312b60a9e1ebfd sio:SIO_000628 miriam-gene:335, lld:C0268380; a sio:SIO_001121 . } dgn-np:NP243390.RAiSQg9b-iTAb2J2EamQy-lAmOaco8t11JLu-nh3Dj9MA130_provenance { dgn-np:NP243390.RAiSQg9b-iTAb2J2EamQy-lAmOaco8t11JLu-nh3Dj9MA130_assertion dcterms:description "[Clinical management and prognosis of patients with systemic amyloidosis depend entirely on correct identification of the fibril protein, such that light chain amyloidosis (AL, previously referred to as 'primary'), the most frequently diagnosed type, is treated with chemotherapy, which has absolutely no role in hereditary apolipoprotein A-I amyloidosis.]. 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:21820994; 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:NP243390.RAiSQg9b-iTAb2J2EamQy-lAmOaco8t11JLu-nh3Dj9MA130_publicationInfo { this: dcterms:created "2015-08-25T14:39:58+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" . }