@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP607749.RAhdCDgF933wVd1BKecO9PmW3MloZXGQuXCZFQuM8Ucb4
> .
@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:NP607749.RAhdCDgF933wVd1BKecO9PmW3MloZXGQuXCZFQuM8Ucb4130_head
{
this:
np:hasAssertion
dgn-np:NP607749.RAhdCDgF933wVd1BKecO9PmW3MloZXGQuXCZFQuM8Ucb4130_assertion
;
np:hasProvenance
dgn-np:NP607749.RAhdCDgF933wVd1BKecO9PmW3MloZXGQuXCZFQuM8Ucb4130_provenance
;
np:hasPublicationInfo
dgn-np:NP607749.RAhdCDgF933wVd1BKecO9PmW3MloZXGQuXCZFQuM8Ucb4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP607749.RAhdCDgF933wVd1BKecO9PmW3MloZXGQuXCZFQuM8Ucb4130_assertion
a
np:Assertion
.
dgn-np:NP607749.RAhdCDgF933wVd1BKecO9PmW3MloZXGQuXCZFQuM8Ucb4130_provenance
a
np:Provenance
.
dgn-np:NP607749.RAhdCDgF933wVd1BKecO9PmW3MloZXGQuXCZFQuM8Ucb4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP607749.RAhdCDgF933wVd1BKecO9PmW3MloZXGQuXCZFQuM8Ucb4130_assertion
{
miriam-gene:2022
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN28d787df1ecd24a0fe7260460c91fec2
sio:SIO_000628
miriam-gene:2022
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP607749.RAhdCDgF933wVd1BKecO9PmW3MloZXGQuXCZFQuM8Ucb4130_provenance
{
dgn-np:NP607749.RAhdCDgF933wVd1BKecO9PmW3MloZXGQuXCZFQuM8Ucb4130_assertion
dcterms:description
"[Furthermore, our study extends previous observations by demonstrating no association between endoglin and either IA or SAH regardless of whether data were stratified for modifiable risk factors such as smoking and hypertension.]. 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:15976502
;
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:NP607749.RAhdCDgF933wVd1BKecO9PmW3MloZXGQuXCZFQuM8Ucb4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:04+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" .
}