@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP882144.RA7M5xxM5oqkxTxRX299fJTR4FJpKu6hYkw_-MSY4Qf4g
> .
@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:NP882144.RA7M5xxM5oqkxTxRX299fJTR4FJpKu6hYkw_-MSY4Qf4g130_head
{
this:
np:hasAssertion
dgn-np:NP882144.RA7M5xxM5oqkxTxRX299fJTR4FJpKu6hYkw_-MSY4Qf4g130_assertion
;
np:hasProvenance
dgn-np:NP882144.RA7M5xxM5oqkxTxRX299fJTR4FJpKu6hYkw_-MSY4Qf4g130_provenance
;
np:hasPublicationInfo
dgn-np:NP882144.RA7M5xxM5oqkxTxRX299fJTR4FJpKu6hYkw_-MSY4Qf4g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP882144.RA7M5xxM5oqkxTxRX299fJTR4FJpKu6hYkw_-MSY4Qf4g130_assertion
a
np:Assertion
.
dgn-np:NP882144.RA7M5xxM5oqkxTxRX299fJTR4FJpKu6hYkw_-MSY4Qf4g130_provenance
a
np:Provenance
.
dgn-np:NP882144.RA7M5xxM5oqkxTxRX299fJTR4FJpKu6hYkw_-MSY4Qf4g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP882144.RA7M5xxM5oqkxTxRX299fJTR4FJpKu6hYkw_-MSY4Qf4g130_assertion
{
miriam-gene:1604
a
ncit:C16612
.
lld:C0002878
a
ncit:C7057
.
dgn-gda:DGNb5ae1841b545796f30a40ca9b2a141d9
sio:SIO_000628
miriam-gene:1604
,
lld:C0002878
;
a
sio:SIO_001121
.
}
dgn-np:NP882144.RA7M5xxM5oqkxTxRX299fJTR4FJpKu6hYkw_-MSY4Qf4g130_provenance
{
dgn-np:NP882144.RA7M5xxM5oqkxTxRX299fJTR4FJpKu6hYkw_-MSY4Qf4g130_assertion
dcterms:description
"[Although the pathogenesis of hemolytic anemia in PNH is related to the absence of CD55 and CD59 molecules on the membrane of red cells, the mechanism responsible for the increased incidence of thrombotic events in PNH is not clear.]. 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:8885138
;
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:NP882144.RA7M5xxM5oqkxTxRX299fJTR4FJpKu6hYkw_-MSY4Qf4g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:59+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" .
}