@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1031470.RArArfL6pXXfaN0XbO7MN1TfG4ssOjbEj5zd0mLexOWrw
> .
@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:NP1031470.RArArfL6pXXfaN0XbO7MN1TfG4ssOjbEj5zd0mLexOWrw130_head
{
this:
np:hasAssertion
dgn-np:NP1031470.RArArfL6pXXfaN0XbO7MN1TfG4ssOjbEj5zd0mLexOWrw130_assertion
;
np:hasProvenance
dgn-np:NP1031470.RArArfL6pXXfaN0XbO7MN1TfG4ssOjbEj5zd0mLexOWrw130_provenance
;
np:hasPublicationInfo
dgn-np:NP1031470.RArArfL6pXXfaN0XbO7MN1TfG4ssOjbEj5zd0mLexOWrw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1031470.RArArfL6pXXfaN0XbO7MN1TfG4ssOjbEj5zd0mLexOWrw130_assertion
a
np:Assertion
.
dgn-np:NP1031470.RArArfL6pXXfaN0XbO7MN1TfG4ssOjbEj5zd0mLexOWrw130_provenance
a
np:Provenance
.
dgn-np:NP1031470.RArArfL6pXXfaN0XbO7MN1TfG4ssOjbEj5zd0mLexOWrw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1031470.RArArfL6pXXfaN0XbO7MN1TfG4ssOjbEj5zd0mLexOWrw130_assertion
{
miriam-gene:7292
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGN0dd811372edff852de49d9016e49d185
sio:SIO_000628
miriam-gene:7292
,
lld:C0027051
;
a
sio:SIO_001122
.
}
dgn-np:NP1031470.RArArfL6pXXfaN0XbO7MN1TfG4ssOjbEj5zd0mLexOWrw130_provenance
{
dgn-np:NP1031470.RArArfL6pXXfaN0XbO7MN1TfG4ssOjbEj5zd0mLexOWrw130_assertion
dcterms:description
"[Recent studies indicate that the single nucleotide polymorphism (SNP) rs3850641 in TNFSF4 is associated with higher risk of myocardial infarction, but little is known about the association between TNFSF4 variation and cerebral infarction (CI).]. 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:23184501
;
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:NP1031470.RArArfL6pXXfaN0XbO7MN1TfG4ssOjbEj5zd0mLexOWrw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:33+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" .
}