@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP716225.RAS194RnPkwm7Vd70FYo8NGbSeQwNvwULVasDSUE-ue08
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP716225.RAS194RnPkwm7Vd70FYo8NGbSeQwNvwULVasDSUE-ue08130_head
{
this:
np:hasAssertion
dgn-np:NP716225.RAS194RnPkwm7Vd70FYo8NGbSeQwNvwULVasDSUE-ue08130_assertion
;
np:hasProvenance
dgn-np:NP716225.RAS194RnPkwm7Vd70FYo8NGbSeQwNvwULVasDSUE-ue08130_provenance
;
np:hasPublicationInfo
dgn-np:NP716225.RAS194RnPkwm7Vd70FYo8NGbSeQwNvwULVasDSUE-ue08130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP716225.RAS194RnPkwm7Vd70FYo8NGbSeQwNvwULVasDSUE-ue08130_assertion
a
np:Assertion
.
dgn-np:NP716225.RAS194RnPkwm7Vd70FYo8NGbSeQwNvwULVasDSUE-ue08130_provenance
a
np:Provenance
.
dgn-np:NP716225.RAS194RnPkwm7Vd70FYo8NGbSeQwNvwULVasDSUE-ue08130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP716225.RAS194RnPkwm7Vd70FYo8NGbSeQwNvwULVasDSUE-ue08130_assertion
{
miriam-gene:3949
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGNf3dec32d58ac07d31a3fc8a8b859c50f
sio:SIO_000628
miriam-gene:3949
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP716225.RAS194RnPkwm7Vd70FYo8NGbSeQwNvwULVasDSUE-ue08130_provenance
{
dgn-np:NP716225.RAS194RnPkwm7Vd70FYo8NGbSeQwNvwULVasDSUE-ue08130_assertion
dcterms:description
"[The considerable variation in age of onset of CHD in patients with FH is believed to arise from conventional risk factors, as well as genetic variation other than in the low-density lipoprotein receptor 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:19166692
;
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:NP716225.RAS194RnPkwm7Vd70FYo8NGbSeQwNvwULVasDSUE-ue08130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:10+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}