@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU
> .
@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:NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU130_head
{
this:
np:hasAssertion
dgn-np:NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU130_assertion
;
np:hasProvenance
dgn-np:NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU130_provenance
;
np:hasPublicationInfo
dgn-np:NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU130_assertion
a
np:Assertion
.
dgn-np:NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU130_provenance
a
np:Provenance
.
dgn-np:NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU130_assertion
{
miriam-gene:356
a
ncit:C16612
.
lld:C0004364
a
ncit:C7057
.
dgn-gda:DGN85d0b5804e0590591ba5f00f9463d1f9
sio:SIO_000628
miriam-gene:356
,
lld:C0004364
;
a
sio:SIO_001121
.
}
dgn-np:NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU130_provenance
{
dgn-np:NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU130_assertion
dcterms:description
"[The presence of risk variants in complement regulatory proteins in patients with SLE and/or APL Ab who develop preeclampsia, as well as in preeclampsia patients lacking autoimmune disease, links complement activation to disease pathogenesis and suggests new targets for treatment of this important public health problem.]. 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:21445332
;
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:NP629495.RAZcuBwehKRtO7pKnRIeNXmOxkMqFlQcpPmbpflivbMbU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:20+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
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"v2.1.0" .
}