@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP166270.RAMl7PPAhSNR4YP-TClgklSQRlOq5VlU_38JIKhhBQ7jk
> .
@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:NP166270.RAMl7PPAhSNR4YP-TClgklSQRlOq5VlU_38JIKhhBQ7jk130_head
{
this:
np:hasAssertion
dgn-np:NP166270.RAMl7PPAhSNR4YP-TClgklSQRlOq5VlU_38JIKhhBQ7jk130_assertion
;
np:hasProvenance
dgn-np:NP166270.RAMl7PPAhSNR4YP-TClgklSQRlOq5VlU_38JIKhhBQ7jk130_provenance
;
np:hasPublicationInfo
dgn-np:NP166270.RAMl7PPAhSNR4YP-TClgklSQRlOq5VlU_38JIKhhBQ7jk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP166270.RAMl7PPAhSNR4YP-TClgklSQRlOq5VlU_38JIKhhBQ7jk130_assertion
a
np:Assertion
.
dgn-np:NP166270.RAMl7PPAhSNR4YP-TClgklSQRlOq5VlU_38JIKhhBQ7jk130_provenance
a
np:Provenance
.
dgn-np:NP166270.RAMl7PPAhSNR4YP-TClgklSQRlOq5VlU_38JIKhhBQ7jk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP166270.RAMl7PPAhSNR4YP-TClgklSQRlOq5VlU_38JIKhhBQ7jk130_assertion
{
miriam-gene:65268
a
ncit:C16612
.
lld:C0038525
a
ncit:C7057
.
dgn-gda:DGNee0b8b102957de52818534eb796ca6d2
sio:SIO_000628
miriam-gene:65268
,
lld:C0038525
;
a
sio:SIO_001122
.
}
dgn-np:NP166270.RAMl7PPAhSNR4YP-TClgklSQRlOq5VlU_38JIKhhBQ7jk130_provenance
{
dgn-np:NP166270.RAMl7PPAhSNR4YP-TClgklSQRlOq5VlU_38JIKhhBQ7jk130_assertion
dcterms:description
"[Genotypes for ERLIN1, TRAPPC9, and WNK2 may prove informative for assessment of the genetic risk for intracerebral hemorrhage, and those for ITM2C and MAPKAP1 may be beneficial in assessment of the genetic risk for subarachnoid hemorrhage in Japanese individuals.]. 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:20198315
;
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:NP166270.RAMl7PPAhSNR4YP-TClgklSQRlOq5VlU_38JIKhhBQ7jk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:02+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" .
}