@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI
> .
@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:NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_head
{
this:
np:hasAssertion
dgn-np:NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_assertion
;
np:hasProvenance
dgn-np:NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_provenance
;
np:hasPublicationInfo
dgn-np:NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_assertion
a
np:Assertion
.
dgn-np:NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_provenance
a
np:Provenance
.
dgn-np:NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_assertion
{
miriam-gene:6098
a
ncit:C16612
.
lld:C0038525
a
ncit:C7057
.
dgn-gda:DGNff0020991f8c83934ac263b16ad619c3
sio:SIO_000628
miriam-gene:6098
,
lld:C0038525
;
a
sio:SIO_001121
.
}
dgn-np:NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_provenance
{
dgn-np:NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_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:NP561466.RAX2L_aOCm4b5ScQ0Ji1lm27XQIP45z8s5B7mv05XNkRI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:38+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" .
}