@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:NP412877.RAsPqKsIFXTofedWpWx20fWeYo32nnCjgm2ptMh5JhITk130_head { this: np:hasAssertion dgn-np:NP412877.RAsPqKsIFXTofedWpWx20fWeYo32nnCjgm2ptMh5JhITk130_assertion; np:hasProvenance dgn-np:NP412877.RAsPqKsIFXTofedWpWx20fWeYo32nnCjgm2ptMh5JhITk130_provenance; np:hasPublicationInfo dgn-np:NP412877.RAsPqKsIFXTofedWpWx20fWeYo32nnCjgm2ptMh5JhITk130_publicationInfo; a np:Nanopublication . dgn-np:NP412877.RAsPqKsIFXTofedWpWx20fWeYo32nnCjgm2ptMh5JhITk130_assertion a np:Assertion . dgn-np:NP412877.RAsPqKsIFXTofedWpWx20fWeYo32nnCjgm2ptMh5JhITk130_provenance a np:Provenance . dgn-np:NP412877.RAsPqKsIFXTofedWpWx20fWeYo32nnCjgm2ptMh5JhITk130_publicationInfo a np:PublicationInfo . } dgn-np:NP412877.RAsPqKsIFXTofedWpWx20fWeYo32nnCjgm2ptMh5JhITk130_assertion { miriam-gene:4023 a ncit:C16612 . lld:C0023817 a ncit:C7057 . dgn-gda:DGNaa03835af2fbe954feca58177430da68 sio:SIO_000628 miriam-gene:4023, lld:C0023817; a sio:SIO_001121 . } dgn-np:NP412877.RAsPqKsIFXTofedWpWx20fWeYo32nnCjgm2ptMh5JhITk130_provenance { dgn-np:NP412877.RAsPqKsIFXTofedWpWx20fWeYo32nnCjgm2ptMh5JhITk130_assertion dcterms:description "[Two of nine subjects with the established diagnosis of FCHL, five of the 14 FCHL clinic patients, and 13 of the 33 CAD subjects with FCHL had reduced LPL activity in the same range as do individuals who are obligate heterozygotes for LPL deficiency.]. 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:1390589; 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:NP412877.RAsPqKsIFXTofedWpWx20fWeYo32nnCjgm2ptMh5JhITk130_publicationInfo { this: dcterms:created "2016-05-13T12:44:52+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" . }