@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP708106.RAg03YtsjVgboazRjWklWBrg5-cU6Pt8wrmHz12z2M_Ts
> .
@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:NP708106.RAg03YtsjVgboazRjWklWBrg5-cU6Pt8wrmHz12z2M_Ts130_head
{
this:
np:hasAssertion
dgn-np:NP708106.RAg03YtsjVgboazRjWklWBrg5-cU6Pt8wrmHz12z2M_Ts130_assertion
;
np:hasProvenance
dgn-np:NP708106.RAg03YtsjVgboazRjWklWBrg5-cU6Pt8wrmHz12z2M_Ts130_provenance
;
np:hasPublicationInfo
dgn-np:NP708106.RAg03YtsjVgboazRjWklWBrg5-cU6Pt8wrmHz12z2M_Ts130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP708106.RAg03YtsjVgboazRjWklWBrg5-cU6Pt8wrmHz12z2M_Ts130_assertion
a
np:Assertion
.
dgn-np:NP708106.RAg03YtsjVgboazRjWklWBrg5-cU6Pt8wrmHz12z2M_Ts130_provenance
a
np:Provenance
.
dgn-np:NP708106.RAg03YtsjVgboazRjWklWBrg5-cU6Pt8wrmHz12z2M_Ts130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP708106.RAg03YtsjVgboazRjWklWBrg5-cU6Pt8wrmHz12z2M_Ts130_assertion
{
miriam-gene:6559
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGNfc908e919320262d7a1db8d97274d30d
sio:SIO_000628
miriam-gene:6559
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP708106.RAg03YtsjVgboazRjWklWBrg5-cU6Pt8wrmHz12z2M_Ts130_provenance
{
dgn-np:NP708106.RAg03YtsjVgboazRjWklWBrg5-cU6Pt8wrmHz12z2M_Ts130_assertion
dcterms:description
"[For this study, given the disrupted family backgrounds of many of our patients and the unreliability of family histories, our hypothesis was that in comparison with other samples, family history of coronary heart disease would be a poor screening tool for the identification of children with elevations in total serum cholesterol (TSC).]. 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:8265303
;
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:NP708106.RAg03YtsjVgboazRjWklWBrg5-cU6Pt8wrmHz12z2M_Ts130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:10+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" .
}