@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP782991.RAc1I7WSY84LKJlSDbgdrx2hVNOW47euL-3Tpcch0XQp4
> .
@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:NP782991.RAc1I7WSY84LKJlSDbgdrx2hVNOW47euL-3Tpcch0XQp4130_head
{
this:
np:hasAssertion
dgn-np:NP782991.RAc1I7WSY84LKJlSDbgdrx2hVNOW47euL-3Tpcch0XQp4130_assertion
;
np:hasProvenance
dgn-np:NP782991.RAc1I7WSY84LKJlSDbgdrx2hVNOW47euL-3Tpcch0XQp4130_provenance
;
np:hasPublicationInfo
dgn-np:NP782991.RAc1I7WSY84LKJlSDbgdrx2hVNOW47euL-3Tpcch0XQp4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP782991.RAc1I7WSY84LKJlSDbgdrx2hVNOW47euL-3Tpcch0XQp4130_assertion
a
np:Assertion
.
dgn-np:NP782991.RAc1I7WSY84LKJlSDbgdrx2hVNOW47euL-3Tpcch0XQp4130_provenance
a
np:Provenance
.
dgn-np:NP782991.RAc1I7WSY84LKJlSDbgdrx2hVNOW47euL-3Tpcch0XQp4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP782991.RAc1I7WSY84LKJlSDbgdrx2hVNOW47euL-3Tpcch0XQp4130_assertion
{
miriam-gene:64240
a
ncit:C16612
.
lld:C0524620
a
ncit:C7057
.
dgn-gda:DGNb680fe524e6979a4ed4ba7448e87a841
sio:SIO_000628
miriam-gene:64240
,
lld:C0524620
;
a
sio:SIO_001121
.
}
dgn-np:NP782991.RAc1I7WSY84LKJlSDbgdrx2hVNOW47euL-3Tpcch0XQp4130_provenance
{
dgn-np:NP782991.RAc1I7WSY84LKJlSDbgdrx2hVNOW47euL-3Tpcch0XQp4130_assertion
dcterms:description
"[Low serum cholesterol and cholesterol absorption were linked to the D19H polymorphism of the ABCG8 gene, and characteristics of the insulin resistance syndrome in men were linked with the Q604E polymorphism of the ABCG5 gene.]. 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:15175352
;
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:NP782991.RAc1I7WSY84LKJlSDbgdrx2hVNOW47euL-3Tpcch0XQp4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:54+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" .
}