@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP757567.RAw4btnV8bHpl4DN0i1BVEiBXSVLPgn-k70s2NBaHvM7E
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP757567.RAw4btnV8bHpl4DN0i1BVEiBXSVLPgn-k70s2NBaHvM7E130_head
{
this:
np:hasAssertion
dgn-np:NP757567.RAw4btnV8bHpl4DN0i1BVEiBXSVLPgn-k70s2NBaHvM7E130_assertion
;
np:hasProvenance
dgn-np:NP757567.RAw4btnV8bHpl4DN0i1BVEiBXSVLPgn-k70s2NBaHvM7E130_provenance
;
np:hasPublicationInfo
dgn-np:NP757567.RAw4btnV8bHpl4DN0i1BVEiBXSVLPgn-k70s2NBaHvM7E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP757567.RAw4btnV8bHpl4DN0i1BVEiBXSVLPgn-k70s2NBaHvM7E130_assertion
a
np:Assertion
.
dgn-np:NP757567.RAw4btnV8bHpl4DN0i1BVEiBXSVLPgn-k70s2NBaHvM7E130_provenance
a
np:Provenance
.
dgn-np:NP757567.RAw4btnV8bHpl4DN0i1BVEiBXSVLPgn-k70s2NBaHvM7E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP757567.RAw4btnV8bHpl4DN0i1BVEiBXSVLPgn-k70s2NBaHvM7E130_assertion
{
miriam-gene:3936
a
ncit:C16612
.
lld:C0020474
a
ncit:C7057
.
dgn-gda:DGN13168ab7f081b6e32b94c46a56c96dff
sio:SIO_000628
miriam-gene:3936
,
lld:C0020474
;
a
sio:SIO_001121
.
}
dgn-np:NP757567.RAw4btnV8bHpl4DN0i1BVEiBXSVLPgn-k70s2NBaHvM7E130_provenance
{
dgn-np:NP757567.RAw4btnV8bHpl4DN0i1BVEiBXSVLPgn-k70s2NBaHvM7E130_assertion
dcterms:description
"[It is considerable clinical relevance that the apoC-III gene may be acting as a modifier gene that is only expressed in the presence of other factors (e.g., increased VLDL flux, low LPL activity) and therefore may predispose those members of FCHL families carrying the T1100 allele to express the FCHL phenotype.]. 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:9215535
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP757567.RAw4btnV8bHpl4DN0i1BVEiBXSVLPgn-k70s2NBaHvM7E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:38+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}