@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP652563.RAQykvrZIVVqQPonZJ_fs-2NLufFy026KV9ZLVwb4HiqU
> .
@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:NP652563.RAQykvrZIVVqQPonZJ_fs-2NLufFy026KV9ZLVwb4HiqU130_head
{
this:
np:hasAssertion
dgn-np:NP652563.RAQykvrZIVVqQPonZJ_fs-2NLufFy026KV9ZLVwb4HiqU130_assertion
;
np:hasProvenance
dgn-np:NP652563.RAQykvrZIVVqQPonZJ_fs-2NLufFy026KV9ZLVwb4HiqU130_provenance
;
np:hasPublicationInfo
dgn-np:NP652563.RAQykvrZIVVqQPonZJ_fs-2NLufFy026KV9ZLVwb4HiqU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP652563.RAQykvrZIVVqQPonZJ_fs-2NLufFy026KV9ZLVwb4HiqU130_assertion
a
np:Assertion
.
dgn-np:NP652563.RAQykvrZIVVqQPonZJ_fs-2NLufFy026KV9ZLVwb4HiqU130_provenance
a
np:Provenance
.
dgn-np:NP652563.RAQykvrZIVVqQPonZJ_fs-2NLufFy026KV9ZLVwb4HiqU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP652563.RAQykvrZIVVqQPonZJ_fs-2NLufFy026KV9ZLVwb4HiqU130_assertion
{
miriam-gene:3423
a
ncit:C16612
.
lld:C0085096
a
ncit:C7057
.
dgn-gda:DGNdf3daf89970dba620ef85db7c5e99c09
sio:SIO_000628
miriam-gene:3423
,
lld:C0085096
;
a
sio:SIO_001121
.
}
dgn-np:NP652563.RAQykvrZIVVqQPonZJ_fs-2NLufFy026KV9ZLVwb4HiqU130_provenance
{
dgn-np:NP652563.RAQykvrZIVVqQPonZJ_fs-2NLufFy026KV9ZLVwb4HiqU130_assertion
dcterms:description
"[A comparison of PVD and clinical case reports indicates that PVD detection in areas with intermediate or high clinical case prevalence may not reach commonly used criteria for triggering testing to IDS.]. 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:18466179
;
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:NP652563.RAQykvrZIVVqQPonZJ_fs-2NLufFy026KV9ZLVwb4HiqU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:33+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" .
}