@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP377361.RAhu252l2IEhKb8utnj1Z5B0bNCKmEOGJnbYg5maEbl1M
> .
@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/v3.0.0/void/
> .
dgn-np:NP377361.RAhu252l2IEhKb8utnj1Z5B0bNCKmEOGJnbYg5maEbl1M130_head
{
this:
np:hasAssertion
dgn-np:NP377361.RAhu252l2IEhKb8utnj1Z5B0bNCKmEOGJnbYg5maEbl1M130_assertion
;
np:hasProvenance
dgn-np:NP377361.RAhu252l2IEhKb8utnj1Z5B0bNCKmEOGJnbYg5maEbl1M130_provenance
;
np:hasPublicationInfo
dgn-np:NP377361.RAhu252l2IEhKb8utnj1Z5B0bNCKmEOGJnbYg5maEbl1M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP377361.RAhu252l2IEhKb8utnj1Z5B0bNCKmEOGJnbYg5maEbl1M130_assertion
a
np:Assertion
.
dgn-np:NP377361.RAhu252l2IEhKb8utnj1Z5B0bNCKmEOGJnbYg5maEbl1M130_provenance
a
np:Provenance
.
dgn-np:NP377361.RAhu252l2IEhKb8utnj1Z5B0bNCKmEOGJnbYg5maEbl1M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP377361.RAhu252l2IEhKb8utnj1Z5B0bNCKmEOGJnbYg5maEbl1M130_assertion
{
miriam-gene:2052
a
ncit:C16612
.
lld:C0013537
a
ncit:C7057
.
dgn-gda:DGNf654fac77c83cad63774d3bff0a7f569
sio:SIO_000628
miriam-gene:2052
,
lld:C0013537
;
a
sio:SIO_001121
.
}
dgn-np:NP377361.RAhu252l2IEhKb8utnj1Z5B0bNCKmEOGJnbYg5maEbl1M130_provenance
{
dgn-np:NP377361.RAhu252l2IEhKb8utnj1Z5B0bNCKmEOGJnbYg5maEbl1M130_assertion
dcterms:description
"[Since EPHX1 is highly expressed in the liver, can interact with various signaling pathways and is involved in central nervous system disorders, the association of EPHX1 polymorphism with the HELLP syndrome and eclampsia may hint to EPHX being a further key player in the pathogenesis of preeclampsia.]. 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:24013430
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP377361.RAhu252l2IEhKb8utnj1Z5B0bNCKmEOGJnbYg5maEbl1M130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:18+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}