@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP240096.RACZ65atsQ28BEdPe8jaPr2XmOEaT7wAP6fxWg1UDwii8
> .
@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:NP240096.RACZ65atsQ28BEdPe8jaPr2XmOEaT7wAP6fxWg1UDwii8130_head
{
this:
np:hasAssertion
dgn-np:NP240096.RACZ65atsQ28BEdPe8jaPr2XmOEaT7wAP6fxWg1UDwii8130_assertion
;
np:hasProvenance
dgn-np:NP240096.RACZ65atsQ28BEdPe8jaPr2XmOEaT7wAP6fxWg1UDwii8130_provenance
;
np:hasPublicationInfo
dgn-np:NP240096.RACZ65atsQ28BEdPe8jaPr2XmOEaT7wAP6fxWg1UDwii8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP240096.RACZ65atsQ28BEdPe8jaPr2XmOEaT7wAP6fxWg1UDwii8130_assertion
a
np:Assertion
.
dgn-np:NP240096.RACZ65atsQ28BEdPe8jaPr2XmOEaT7wAP6fxWg1UDwii8130_provenance
a
np:Provenance
.
dgn-np:NP240096.RACZ65atsQ28BEdPe8jaPr2XmOEaT7wAP6fxWg1UDwii8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP240096.RACZ65atsQ28BEdPe8jaPr2XmOEaT7wAP6fxWg1UDwii8130_assertion
{
miriam-gene:59271
a
ncit:C16612
.
lld:C1959635
a
ncit:C7057
.
dgn-gda:DGN13a32e022ef4a3f74bb9370c64ab6dc1
sio:SIO_000628
miriam-gene:59271
,
lld:C1959635
;
a
sio:SIO_001121
.
}
dgn-np:NP240096.RACZ65atsQ28BEdPe8jaPr2XmOEaT7wAP6fxWg1UDwii8130_provenance
{
dgn-np:NP240096.RACZ65atsQ28BEdPe8jaPr2XmOEaT7wAP6fxWg1UDwii8130_assertion
dcterms:description
"[Late (third-trimester) cases of `idiopathic` NIHF are likely to be negative by all methods, either because they are not attributable to PV infection or because PV protein and DNA are below detectable levels or are no longer present.]. 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:9670826
;
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:NP240096.RACZ65atsQ28BEdPe8jaPr2XmOEaT7wAP6fxWg1UDwii8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:14+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" .
}