@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP480706.RAsqhXfalf4U7oBHjW_Eh2AI2YYBzIato4ehUJZqth4v4
> .
@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:NP480706.RAsqhXfalf4U7oBHjW_Eh2AI2YYBzIato4ehUJZqth4v4130_head
{
this:
np:hasAssertion
dgn-np:NP480706.RAsqhXfalf4U7oBHjW_Eh2AI2YYBzIato4ehUJZqth4v4130_assertion
;
np:hasProvenance
dgn-np:NP480706.RAsqhXfalf4U7oBHjW_Eh2AI2YYBzIato4ehUJZqth4v4130_provenance
;
np:hasPublicationInfo
dgn-np:NP480706.RAsqhXfalf4U7oBHjW_Eh2AI2YYBzIato4ehUJZqth4v4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP480706.RAsqhXfalf4U7oBHjW_Eh2AI2YYBzIato4ehUJZqth4v4130_assertion
a
np:Assertion
.
dgn-np:NP480706.RAsqhXfalf4U7oBHjW_Eh2AI2YYBzIato4ehUJZqth4v4130_provenance
a
np:Provenance
.
dgn-np:NP480706.RAsqhXfalf4U7oBHjW_Eh2AI2YYBzIato4ehUJZqth4v4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP480706.RAsqhXfalf4U7oBHjW_Eh2AI2YYBzIato4ehUJZqth4v4130_assertion
{
miriam-gene:1281
a
ncit:C16612
.
lld:C0007766
a
ncit:C7057
.
dgn-gda:DGN60a3b9738f43e741acfd27d1e70166d8
sio:SIO_000628
miriam-gene:1281
,
lld:C0007766
;
a
sio:SIO_001121
.
}
dgn-np:NP480706.RAsqhXfalf4U7oBHjW_Eh2AI2YYBzIato4ehUJZqth4v4130_provenance
{
dgn-np:NP480706.RAsqhXfalf4U7oBHjW_Eh2AI2YYBzIato4ehUJZqth4v4130_assertion
dcterms:description
"[To study whether COL3A1 variants are associated with sporadic IAs, the association of COL3A1 variants with sporadic IAs was tested in 298 cases and 488 controls, replicated in an independent population of 192 cases and 1,690 controls, and further verified in 633 patients with intra-cerebral hemorrhage, 1,074 hypertensives, and 1,883 controls.]. 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:22241462
;
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:NP480706.RAsqhXfalf4U7oBHjW_Eh2AI2YYBzIato4ehUJZqth4v4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:47+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: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" .
}