@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk
> .
@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:NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_head
{
this:
np:hasAssertion
dgn-np:NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_assertion
;
np:hasProvenance
dgn-np:NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_provenance
;
np:hasPublicationInfo
dgn-np:NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_assertion
a
np:Assertion
.
dgn-np:NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_provenance
a
np:Provenance
.
dgn-np:NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0020445
a
ncit:C7057
.
dgn-gda:DGN5492bbe98d9da265a1a70162884e153f
sio:SIO_000628
miriam-gene:348
,
lld:C0020445
;
a
sio:SIO_001121
.
}
dgn-np:NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_provenance
{
dgn-np:NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_assertion
dcterms:description
"[Similar to its existing use in the diagnosis of monogenic dyslipidemias such as familial hypercholesterolemia, clinical inquiry regarding family history was identified as an important determinant of eligibility for APOE genotyping performed in the context of chronic disease risk management.]. 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:25731628
;
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:NP1267486.RAEQoCW2J56rqm3Ykv_RGlPNcpWfQjOkFugeG1AapqRBk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:20+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" .
}