@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:NP1245970.RAKtXMO2mJiK2h7MWhM8hPiH_QlcwcLg-LXKfLsuCcOEU130_head { this: np:hasAssertion dgn-np:NP1245970.RAKtXMO2mJiK2h7MWhM8hPiH_QlcwcLg-LXKfLsuCcOEU130_assertion; np:hasProvenance dgn-np:NP1245970.RAKtXMO2mJiK2h7MWhM8hPiH_QlcwcLg-LXKfLsuCcOEU130_provenance; np:hasPublicationInfo dgn-np:NP1245970.RAKtXMO2mJiK2h7MWhM8hPiH_QlcwcLg-LXKfLsuCcOEU130_publicationInfo; a np:Nanopublication . dgn-np:NP1245970.RAKtXMO2mJiK2h7MWhM8hPiH_QlcwcLg-LXKfLsuCcOEU130_assertion a np:Assertion . dgn-np:NP1245970.RAKtXMO2mJiK2h7MWhM8hPiH_QlcwcLg-LXKfLsuCcOEU130_provenance a np:Provenance . dgn-np:NP1245970.RAKtXMO2mJiK2h7MWhM8hPiH_QlcwcLg-LXKfLsuCcOEU130_publicationInfo a np:PublicationInfo . } dgn-np:NP1245970.RAKtXMO2mJiK2h7MWhM8hPiH_QlcwcLg-LXKfLsuCcOEU130_assertion { miriam-gene:7341 a ncit:C16612 . lld:C0024419 a ncit:C7057 . dgn-gda:DGN6a0ff4d0da9fc43dbfe364919fb0f3a0 sio:SIO_000628 miriam-gene:7341, lld:C0024419; a sio:SIO_001121 . } dgn-np:NP1245970.RAKtXMO2mJiK2h7MWhM8hPiH_QlcwcLg-LXKfLsuCcOEU130_provenance { dgn-np:NP1245970.RAKtXMO2mJiK2h7MWhM8hPiH_QlcwcLg-LXKfLsuCcOEU130_assertion dcterms:description "[This study demonstrates that harboring HSP90-SUMO1 identifies healthy individuals at risk for plasma cell dyscrasias and that dominant inheritance of posttranslationally modified autoantigenic paratargs is one of the strongest molecular defined risk factors for MGUS, MM, and WM.]. 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:25485683; 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:NP1245970.RAKtXMO2mJiK2h7MWhM8hPiH_QlcwcLg-LXKfLsuCcOEU130_publicationInfo { this: dcterms:created "2016-05-13T12:51:10+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" . }