@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP378236.RA8vccimZvtQ_fqkvwsOL8JY85d9Yqm5sePmQAAwKh8O4
> .
@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:NP378236.RA8vccimZvtQ_fqkvwsOL8JY85d9Yqm5sePmQAAwKh8O4130_head
{
this:
np:hasAssertion
dgn-np:NP378236.RA8vccimZvtQ_fqkvwsOL8JY85d9Yqm5sePmQAAwKh8O4130_assertion
;
np:hasProvenance
dgn-np:NP378236.RA8vccimZvtQ_fqkvwsOL8JY85d9Yqm5sePmQAAwKh8O4130_provenance
;
np:hasPublicationInfo
dgn-np:NP378236.RA8vccimZvtQ_fqkvwsOL8JY85d9Yqm5sePmQAAwKh8O4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP378236.RA8vccimZvtQ_fqkvwsOL8JY85d9Yqm5sePmQAAwKh8O4130_assertion
a
np:Assertion
.
dgn-np:NP378236.RA8vccimZvtQ_fqkvwsOL8JY85d9Yqm5sePmQAAwKh8O4130_provenance
a
np:Provenance
.
dgn-np:NP378236.RA8vccimZvtQ_fqkvwsOL8JY85d9Yqm5sePmQAAwKh8O4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP378236.RA8vccimZvtQ_fqkvwsOL8JY85d9Yqm5sePmQAAwKh8O4130_assertion
{
miriam-gene:1437
a
ncit:C16612
.
lld:C0007682
a
ncit:C7057
.
dgn-gda:DGN38a0b84514f9ac6fa11dc58f6cef3380
sio:SIO_000628
miriam-gene:1437
,
lld:C0007682
;
a
sio:SIO_001121
.
}
dgn-np:NP378236.RA8vccimZvtQ_fqkvwsOL8JY85d9Yqm5sePmQAAwKh8O4130_provenance
{
dgn-np:NP378236.RA8vccimZvtQ_fqkvwsOL8JY85d9Yqm5sePmQAAwKh8O4130_assertion
dcterms:description
"[This study indicates that the detection of HCMV pp67 mRNA in CSF has good correlation with active HCMV CNS disease, whereas CSF culture is insensitive and qualitative DNA PCR may detect latent nonreplicating virus in CSF from patients without HCMV CNS disease.]. 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:10790122
;
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:NP378236.RA8vccimZvtQ_fqkvwsOL8JY85d9Yqm5sePmQAAwKh8O4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:41+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" .
}