@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP831187.RAAqvIjMvBFchKbAa_UXnYbXWknpKCKlICZVj7klAMqqk
> .
@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:NP831187.RAAqvIjMvBFchKbAa_UXnYbXWknpKCKlICZVj7klAMqqk130_head
{
this:
np:hasAssertion
dgn-np:NP831187.RAAqvIjMvBFchKbAa_UXnYbXWknpKCKlICZVj7klAMqqk130_assertion
;
np:hasProvenance
dgn-np:NP831187.RAAqvIjMvBFchKbAa_UXnYbXWknpKCKlICZVj7klAMqqk130_provenance
;
np:hasPublicationInfo
dgn-np:NP831187.RAAqvIjMvBFchKbAa_UXnYbXWknpKCKlICZVj7klAMqqk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP831187.RAAqvIjMvBFchKbAa_UXnYbXWknpKCKlICZVj7klAMqqk130_assertion
a
np:Assertion
.
dgn-np:NP831187.RAAqvIjMvBFchKbAa_UXnYbXWknpKCKlICZVj7klAMqqk130_provenance
a
np:Provenance
.
dgn-np:NP831187.RAAqvIjMvBFchKbAa_UXnYbXWknpKCKlICZVj7klAMqqk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP831187.RAAqvIjMvBFchKbAa_UXnYbXWknpKCKlICZVj7klAMqqk130_assertion
{
miriam-gene:302
a
ncit:C16612
.
lld:C0085278
a
ncit:C7057
.
dgn-gda:DGNfa79b29de38228516fbded3b02adabb9
sio:SIO_000628
miriam-gene:302
,
lld:C0085278
;
a
sio:SIO_001121
.
}
dgn-np:NP831187.RAAqvIjMvBFchKbAa_UXnYbXWknpKCKlICZVj7klAMqqk130_provenance
{
dgn-np:NP831187.RAAqvIjMvBFchKbAa_UXnYbXWknpKCKlICZVj7klAMqqk130_assertion
dcterms:description
"[Over-expression of A2 is seen in acute promyelocytic leukemia during the early hemorrhagic phase, while high titer antibodies to A2, as in antiphospholipid syndrome or cerebral venous thrombosis, are associated with thrombosis.]. 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:21440088
;
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:NP831187.RAAqvIjMvBFchKbAa_UXnYbXWknpKCKlICZVj7klAMqqk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:28+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" .
}