@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP583482.RAanZVwZHxeGlPMhez-MQ727B1Fw4rCw72Zb8ymwxGIbU
> .
@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:NP583482.RAanZVwZHxeGlPMhez-MQ727B1Fw4rCw72Zb8ymwxGIbU130_head
{
this:
np:hasAssertion
dgn-np:NP583482.RAanZVwZHxeGlPMhez-MQ727B1Fw4rCw72Zb8ymwxGIbU130_assertion
;
np:hasProvenance
dgn-np:NP583482.RAanZVwZHxeGlPMhez-MQ727B1Fw4rCw72Zb8ymwxGIbU130_provenance
;
np:hasPublicationInfo
dgn-np:NP583482.RAanZVwZHxeGlPMhez-MQ727B1Fw4rCw72Zb8ymwxGIbU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP583482.RAanZVwZHxeGlPMhez-MQ727B1Fw4rCw72Zb8ymwxGIbU130_assertion
a
np:Assertion
.
dgn-np:NP583482.RAanZVwZHxeGlPMhez-MQ727B1Fw4rCw72Zb8ymwxGIbU130_provenance
a
np:Provenance
.
dgn-np:NP583482.RAanZVwZHxeGlPMhez-MQ727B1Fw4rCw72Zb8ymwxGIbU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP583482.RAanZVwZHxeGlPMhez-MQ727B1Fw4rCw72Zb8ymwxGIbU130_assertion
{
miriam-gene:19
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGN685e73d07da38eebc8c9eb4a2b40b55e
sio:SIO_000628
miriam-gene:19
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP583482.RAanZVwZHxeGlPMhez-MQ727B1Fw4rCw72Zb8ymwxGIbU130_provenance
{
dgn-np:NP583482.RAanZVwZHxeGlPMhez-MQ727B1Fw4rCw72Zb8ymwxGIbU130_assertion
dcterms:description
"[Genotypes for ABCA1, IRAK1, and ROS1 may prove useful for assessment of the genetic risk for atherothrombotic cerebral infarction, whereas those for LIMK1 and CYP3A4 may be similarly beneficial in assessment of the genetic risk for intracerebral hemorrhage and subarachnoid hemorrhage, respectively.]. 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:18566305
;
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 .
}
dgn-np:NP583482.RAanZVwZHxeGlPMhez-MQ727B1Fw4rCw72Zb8ymwxGIbU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:51+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
pav:version
"v2.1.0" .
}