@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP95899.RABacVZExJfSAhXNRe3onEl_ZoBbBGP4U8tgPHOpWd8bo
> .
@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:NP95899.RABacVZExJfSAhXNRe3onEl_ZoBbBGP4U8tgPHOpWd8bo130_head
{
this:
np:hasAssertion
dgn-np:NP95899.RABacVZExJfSAhXNRe3onEl_ZoBbBGP4U8tgPHOpWd8bo130_assertion
;
np:hasProvenance
dgn-np:NP95899.RABacVZExJfSAhXNRe3onEl_ZoBbBGP4U8tgPHOpWd8bo130_provenance
;
np:hasPublicationInfo
dgn-np:NP95899.RABacVZExJfSAhXNRe3onEl_ZoBbBGP4U8tgPHOpWd8bo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP95899.RABacVZExJfSAhXNRe3onEl_ZoBbBGP4U8tgPHOpWd8bo130_assertion
a
np:Assertion
.
dgn-np:NP95899.RABacVZExJfSAhXNRe3onEl_ZoBbBGP4U8tgPHOpWd8bo130_provenance
a
np:Provenance
.
dgn-np:NP95899.RABacVZExJfSAhXNRe3onEl_ZoBbBGP4U8tgPHOpWd8bo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP95899.RABacVZExJfSAhXNRe3onEl_ZoBbBGP4U8tgPHOpWd8bo130_assertion
{
miriam-gene:4318
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGN449f57a92894c6d89c08b25e47769b5d
sio:SIO_000628
miriam-gene:4318
,
lld:C0027051
;
a
sio:SIO_001122
.
}
dgn-np:NP95899.RABacVZExJfSAhXNRe3onEl_ZoBbBGP4U8tgPHOpWd8bo130_provenance
{
dgn-np:NP95899.RABacVZExJfSAhXNRe3onEl_ZoBbBGP4U8tgPHOpWd8bo130_assertion
dcterms:description
"[ Obviously, the gelatinase B C((-1562))T gene polymorphism is not a risk indicator for CAD and MI. With respect to the extent of CHD, the impact of this gene variation may be restricted to individuals with high apolipoprotein B, lipoprotein (a) and/or fib]. 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:16179285
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP95899.RABacVZExJfSAhXNRe3onEl_ZoBbBGP4U8tgPHOpWd8bo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:31+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
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;
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" .
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pav:version
"v4.0.0" .
}