@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:NP1376178.RAMknD98_-AWiXOr0rChTRaLVDhd4b1D14Kw_It11LNGk130_head { this: np:hasAssertion dgn-np:NP1376178.RAMknD98_-AWiXOr0rChTRaLVDhd4b1D14Kw_It11LNGk130_assertion; np:hasProvenance dgn-np:NP1376178.RAMknD98_-AWiXOr0rChTRaLVDhd4b1D14Kw_It11LNGk130_provenance; np:hasPublicationInfo dgn-np:NP1376178.RAMknD98_-AWiXOr0rChTRaLVDhd4b1D14Kw_It11LNGk130_publicationInfo; a np:Nanopublication . dgn-np:NP1376178.RAMknD98_-AWiXOr0rChTRaLVDhd4b1D14Kw_It11LNGk130_assertion a np:Assertion . dgn-np:NP1376178.RAMknD98_-AWiXOr0rChTRaLVDhd4b1D14Kw_It11LNGk130_provenance a np:Provenance . dgn-np:NP1376178.RAMknD98_-AWiXOr0rChTRaLVDhd4b1D14Kw_It11LNGk130_publicationInfo a np:PublicationInfo . } dgn-np:NP1376178.RAMknD98_-AWiXOr0rChTRaLVDhd4b1D14Kw_It11LNGk130_assertion { miriam-gene:4023 a ncit:C16612 . lld:C0020480 a ncit:C7057 . dgn-gda:DGN16d7c622ffb12b8525005766f9a3b721 sio:SIO_000628 miriam-gene:4023, lld:C0020480; a sio:SIO_001121 . } dgn-np:NP1376178.RAMknD98_-AWiXOr0rChTRaLVDhd4b1D14Kw_It11LNGk130_provenance { dgn-np:NP1376178.RAMknD98_-AWiXOr0rChTRaLVDhd4b1D14Kw_It11LNGk130_assertion dcterms:description "[The purpose of this study was to develop an improved method of direct DNA sequencing, which makes it possible to identify heterozygous mutations of the lipoprotein lipase (LPL) gene in order to understand the underlying genetic disorder of type IV hyperlipoproteinemia.]. 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:9209790; 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:NP1376178.RAMknD98_-AWiXOr0rChTRaLVDhd4b1D14Kw_It11LNGk130_publicationInfo { this: dcterms:created "2016-05-13T12:52:09+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" . }