@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ
> .
@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:NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ130_head
{
this:
np:hasAssertion
dgn-np:NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ130_assertion
;
np:hasProvenance
dgn-np:NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ130_assertion
a
np:Assertion
.
dgn-np:NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ130_provenance
a
np:Provenance
.
dgn-np:NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ130_assertion
{
miriam-gene:3949
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGN0c7983877b9ff21f1bd155160a1d53b1
sio:SIO_000628
miriam-gene:3949
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ130_provenance
{
dgn-np:NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ130_assertion
dcterms:description
"[This disease, which is due to mutation in the low density lipoprotein (LDL) receptor gene and results in deficiency of the LDL receptor, is associated with hypercholesterolemia and premature development of coronary heart disease.]. 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:12119548
;
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:NP361381.RAsq8MVtVLEqcXnV4HpSbQ7H38G7ZZAkj5ahd66X_RqRQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:29+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" .
}