@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP898315.RA6Hzmf66w3Ftve6yJjudQD35ZLsYCJs1t9vTCqgmym58
> .
@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:NP898315.RA6Hzmf66w3Ftve6yJjudQD35ZLsYCJs1t9vTCqgmym58130_head
{
this:
np:hasAssertion
dgn-np:NP898315.RA6Hzmf66w3Ftve6yJjudQD35ZLsYCJs1t9vTCqgmym58130_assertion
;
np:hasProvenance
dgn-np:NP898315.RA6Hzmf66w3Ftve6yJjudQD35ZLsYCJs1t9vTCqgmym58130_provenance
;
np:hasPublicationInfo
dgn-np:NP898315.RA6Hzmf66w3Ftve6yJjudQD35ZLsYCJs1t9vTCqgmym58130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP898315.RA6Hzmf66w3Ftve6yJjudQD35ZLsYCJs1t9vTCqgmym58130_assertion
a
np:Assertion
.
dgn-np:NP898315.RA6Hzmf66w3Ftve6yJjudQD35ZLsYCJs1t9vTCqgmym58130_provenance
a
np:Provenance
.
dgn-np:NP898315.RA6Hzmf66w3Ftve6yJjudQD35ZLsYCJs1t9vTCqgmym58130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP898315.RA6Hzmf66w3Ftve6yJjudQD35ZLsYCJs1t9vTCqgmym58130_assertion
{
miriam-gene:4810
a
ncit:C16612
.
lld:C0015230
a
ncit:C7057
.
dgn-gda:DGN1c6773edc90f6f001d30feb3e934c4d7
sio:SIO_000628
miriam-gene:4810
,
lld:C0015230
;
a
sio:SIO_001121
.
}
dgn-np:NP898315.RA6Hzmf66w3Ftve6yJjudQD35ZLsYCJs1t9vTCqgmym58130_provenance
{
dgn-np:NP898315.RA6Hzmf66w3Ftve6yJjudQD35ZLsYCJs1t9vTCqgmym58130_assertion
dcterms:description
"[The goal of this study was to compare newborn dried blood spots from Minnesota infants who had failed NHS, and were designated for referral, with control infants who passed NHS, for the presence of CMV DNA by real-time PCR, using hybridization probes for the CMV gene UL54.]. 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:19820425
;
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:NP898315.RA6Hzmf66w3Ftve6yJjudQD35ZLsYCJs1t9vTCqgmym58130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:12+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" .
}