@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1195137.RAhwASqc3lIn_Gndt4MwCYAijYsv06EXRhzwRGCZZWifY
> .
@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:NP1195137.RAhwASqc3lIn_Gndt4MwCYAijYsv06EXRhzwRGCZZWifY130_head
{
this:
np:hasAssertion
dgn-np:NP1195137.RAhwASqc3lIn_Gndt4MwCYAijYsv06EXRhzwRGCZZWifY130_assertion
;
np:hasProvenance
dgn-np:NP1195137.RAhwASqc3lIn_Gndt4MwCYAijYsv06EXRhzwRGCZZWifY130_provenance
;
np:hasPublicationInfo
dgn-np:NP1195137.RAhwASqc3lIn_Gndt4MwCYAijYsv06EXRhzwRGCZZWifY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1195137.RAhwASqc3lIn_Gndt4MwCYAijYsv06EXRhzwRGCZZWifY130_assertion
a
np:Assertion
.
dgn-np:NP1195137.RAhwASqc3lIn_Gndt4MwCYAijYsv06EXRhzwRGCZZWifY130_provenance
a
np:Provenance
.
dgn-np:NP1195137.RAhwASqc3lIn_Gndt4MwCYAijYsv06EXRhzwRGCZZWifY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1195137.RAhwASqc3lIn_Gndt4MwCYAijYsv06EXRhzwRGCZZWifY130_assertion
{
miriam-gene:4815
a
ncit:C16612
.
lld:C0004153
a
ncit:C7057
.
dgn-gda:DGN32b9c7e8561d423c20b4273974b09656
sio:SIO_000628
miriam-gene:4815
,
lld:C0004153
;
a
sio:SIO_001121
.
}
dgn-np:NP1195137.RAhwASqc3lIn_Gndt4MwCYAijYsv06EXRhzwRGCZZWifY130_provenance
{
dgn-np:NP1195137.RAhwASqc3lIn_Gndt4MwCYAijYsv06EXRhzwRGCZZWifY130_assertion
dcterms:description
"[We sequenced 196 kb around NINJ2 on chromosome 12p13 among 3,986 European ancestry participants, including 475 ischemic stroke cases, from the Atherosclerosis Risk in Communities Study, Cardiovascular Health Study, and Framingham Heart Study.]. 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:24959832
;
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:NP1195137.RAhwASqc3lIn_Gndt4MwCYAijYsv06EXRhzwRGCZZWifY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:47+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" .
}