@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP388166.RAW2ulENwrldg7zFEqarFqTx7DjFZuD36eth2BR8CZHgo
> .
@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:NP388166.RAW2ulENwrldg7zFEqarFqTx7DjFZuD36eth2BR8CZHgo130_head
{
this:
np:hasAssertion
dgn-np:NP388166.RAW2ulENwrldg7zFEqarFqTx7DjFZuD36eth2BR8CZHgo130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP388166.RAW2ulENwrldg7zFEqarFqTx7DjFZuD36eth2BR8CZHgo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP388166.RAW2ulENwrldg7zFEqarFqTx7DjFZuD36eth2BR8CZHgo130_assertion
a
np:Assertion
.
dgn-np:NP388166.RAW2ulENwrldg7zFEqarFqTx7DjFZuD36eth2BR8CZHgo130_provenance
a
np:Provenance
.
dgn-np:NP388166.RAW2ulENwrldg7zFEqarFqTx7DjFZuD36eth2BR8CZHgo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP388166.RAW2ulENwrldg7zFEqarFqTx7DjFZuD36eth2BR8CZHgo130_assertion
{
miriam-gene:3949
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN1fd5ba5b5a8d27c72d4e838cf2f2aa59
sio:SIO_000628
miriam-gene:3949
,
lld:C0010054
;
a
sio:SIO_001121
.
}
dgn-np:NP388166.RAW2ulENwrldg7zFEqarFqTx7DjFZuD36eth2BR8CZHgo130_provenance
{
dgn-np:NP388166.RAW2ulENwrldg7zFEqarFqTx7DjFZuD36eth2BR8CZHgo130_assertion
dcterms:description
"[The aim of this study was to detect mutations in the genes coding for the low-density lipoprotein receptor and apolipoprotein B in patients of Southeast Asian origin with clinically diagnosed familial hypercholesterolemia (FH) and to relate these findings with the observed lower incidence of coronary heart disease in this part of the world.]. 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:11005141
;
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 .
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dgn-np:NP388166.RAW2ulENwrldg7zFEqarFqTx7DjFZuD36eth2BR8CZHgo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:51+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
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"v2.1.0" .
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