@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:NP973519.RA-XHbm9SliAQOiH5yCjGzf-ewEeGmyQ2V0yUFABBxS0w130_head { this: np:hasAssertion dgn-np:NP973519.RA-XHbm9SliAQOiH5yCjGzf-ewEeGmyQ2V0yUFABBxS0w130_assertion; np:hasProvenance dgn-np:NP973519.RA-XHbm9SliAQOiH5yCjGzf-ewEeGmyQ2V0yUFABBxS0w130_provenance; np:hasPublicationInfo dgn-np:NP973519.RA-XHbm9SliAQOiH5yCjGzf-ewEeGmyQ2V0yUFABBxS0w130_publicationInfo; a np:Nanopublication . dgn-np:NP973519.RA-XHbm9SliAQOiH5yCjGzf-ewEeGmyQ2V0yUFABBxS0w130_assertion a np:Assertion . dgn-np:NP973519.RA-XHbm9SliAQOiH5yCjGzf-ewEeGmyQ2V0yUFABBxS0w130_provenance a np:Provenance . dgn-np:NP973519.RA-XHbm9SliAQOiH5yCjGzf-ewEeGmyQ2V0yUFABBxS0w130_publicationInfo a np:PublicationInfo . } dgn-np:NP973519.RA-XHbm9SliAQOiH5yCjGzf-ewEeGmyQ2V0yUFABBxS0w130_assertion { miriam-gene:140913 a ncit:C16612 . lld:C0007222 a ncit:C7057 . dgn-gda:DGN958da72526b277a765f0d078a2aa9d58 sio:SIO_000628 miriam-gene:140913, lld:C0007222; a sio:SIO_001122 . } dgn-np:NP973519.RA-XHbm9SliAQOiH5yCjGzf-ewEeGmyQ2V0yUFABBxS0w130_provenance { dgn-np:NP973519.RA-XHbm9SliAQOiH5yCjGzf-ewEeGmyQ2V0yUFABBxS0w130_assertion dcterms:description "[In a cohort of 258 (161 males) ESRD patients starting renal replacement therapy [glomerular filtration rate (GFR) 6.8 +/- 0.2 mL/min] aged 52 +/- 1 years the following parameters were studied: presence of malnutrition (subjective global assessment), comorbidity [diabetes mellitus and clinical manifest cardiovascular disease (CVD)], carotid plaques (N= 101), hs-CRP, fetuin-A, S-albumin, interleukin (IL)-6, and single nucleotide polymorphisms (SNPs) in the AHSG gene (N= 215) at amino acid positions Thr248Met (C-->T), Thr256Ser (C-->G), Asp276Asn (G-->A), and Arg317Cys (C-->T).]. 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:15882283; 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:NP973519.RA-XHbm9SliAQOiH5yCjGzf-ewEeGmyQ2V0yUFABBxS0w130_publicationInfo { this: dcterms:created "2015-08-25T14:47:34+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" . }