@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP719209.RAox2z8EW20U2Y-WQUuYKzrqilpiWdruz6YTg7d41QOOA
> .
@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:NP719209.RAox2z8EW20U2Y-WQUuYKzrqilpiWdruz6YTg7d41QOOA130_head
{
this:
np:hasAssertion
dgn-np:NP719209.RAox2z8EW20U2Y-WQUuYKzrqilpiWdruz6YTg7d41QOOA130_assertion
;
np:hasProvenance
dgn-np:NP719209.RAox2z8EW20U2Y-WQUuYKzrqilpiWdruz6YTg7d41QOOA130_provenance
;
np:hasPublicationInfo
dgn-np:NP719209.RAox2z8EW20U2Y-WQUuYKzrqilpiWdruz6YTg7d41QOOA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP719209.RAox2z8EW20U2Y-WQUuYKzrqilpiWdruz6YTg7d41QOOA130_assertion
a
np:Assertion
.
dgn-np:NP719209.RAox2z8EW20U2Y-WQUuYKzrqilpiWdruz6YTg7d41QOOA130_provenance
a
np:Provenance
.
dgn-np:NP719209.RAox2z8EW20U2Y-WQUuYKzrqilpiWdruz6YTg7d41QOOA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP719209.RAox2z8EW20U2Y-WQUuYKzrqilpiWdruz6YTg7d41QOOA130_assertion
{
miriam-gene:4810
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGNd43e7af65d4cd3fe592da3df53a84a4a
sio:SIO_000628
miriam-gene:4810
,
lld:C0028754
;
a
sio:SIO_001121
.
}
dgn-np:NP719209.RAox2z8EW20U2Y-WQUuYKzrqilpiWdruz6YTg7d41QOOA130_provenance
{
dgn-np:NP719209.RAox2z8EW20U2Y-WQUuYKzrqilpiWdruz6YTg7d41QOOA130_assertion
dcterms:description
"[There was a suggestion that the associations of the S447X variant with plasma lipids and CHD risk were more pronounced in obese individuals in the NHS study, but this finding was not consistent across the studies.]. 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:19185650
;
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:NP719209.RAox2z8EW20U2Y-WQUuYKzrqilpiWdruz6YTg7d41QOOA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:17+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" .
}