@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP721313.RAOe8N0cC1cJnyEUPfrSyvwhvH8GUspcyi2x67PWkLy_k
> .
@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:NP721313.RAOe8N0cC1cJnyEUPfrSyvwhvH8GUspcyi2x67PWkLy_k130_head
{
this:
np:hasAssertion
dgn-np:NP721313.RAOe8N0cC1cJnyEUPfrSyvwhvH8GUspcyi2x67PWkLy_k130_assertion
;
np:hasProvenance
dgn-np:NP721313.RAOe8N0cC1cJnyEUPfrSyvwhvH8GUspcyi2x67PWkLy_k130_provenance
;
np:hasPublicationInfo
dgn-np:NP721313.RAOe8N0cC1cJnyEUPfrSyvwhvH8GUspcyi2x67PWkLy_k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP721313.RAOe8N0cC1cJnyEUPfrSyvwhvH8GUspcyi2x67PWkLy_k130_assertion
a
np:Assertion
.
dgn-np:NP721313.RAOe8N0cC1cJnyEUPfrSyvwhvH8GUspcyi2x67PWkLy_k130_provenance
a
np:Provenance
.
dgn-np:NP721313.RAOe8N0cC1cJnyEUPfrSyvwhvH8GUspcyi2x67PWkLy_k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP721313.RAOe8N0cC1cJnyEUPfrSyvwhvH8GUspcyi2x67PWkLy_k130_assertion
{
miriam-gene:368
a
ncit:C16612
.
lld:C1859727
a
ncit:C7057
.
dgn-gda:DGN5d8daa773f0ae4021329827714bf7f25
sio:SIO_000628
miriam-gene:368
,
lld:C1859727
;
a
sio:SIO_001121
.
}
dgn-np:NP721313.RAOe8N0cC1cJnyEUPfrSyvwhvH8GUspcyi2x67PWkLy_k130_provenance
{
dgn-np:NP721313.RAOe8N0cC1cJnyEUPfrSyvwhvH8GUspcyi2x67PWkLy_k130_assertion
dcterms:description
"[Monogenic ENPP1, CD73, and ABCC6 deficiencies each drive a molecular pathophysiology of closely related but phenotypically different diseases (generalized arterial calcification of infancy (GACI), pseudoxanthoma elasticum (PXE) and arterial calcification caused by CD73 deficiency (ACDC)), in which premature onset arterial calcification is a prominent but not the sole feature.]. 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:21852556
;
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:NP721313.RAOe8N0cC1cJnyEUPfrSyvwhvH8GUspcyi2x67PWkLy_k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:18+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: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" .
}