@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP233034.RAOopHSAb4dq3_Wk92ZkOc3hJpDMYwI3Uh2lvTUA0091g
> .
@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:NP233034.RAOopHSAb4dq3_Wk92ZkOc3hJpDMYwI3Uh2lvTUA0091g130_head
{
this:
np:hasAssertion
dgn-np:NP233034.RAOopHSAb4dq3_Wk92ZkOc3hJpDMYwI3Uh2lvTUA0091g130_assertion
;
np:hasProvenance
dgn-np:NP233034.RAOopHSAb4dq3_Wk92ZkOc3hJpDMYwI3Uh2lvTUA0091g130_provenance
;
np:hasPublicationInfo
dgn-np:NP233034.RAOopHSAb4dq3_Wk92ZkOc3hJpDMYwI3Uh2lvTUA0091g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP233034.RAOopHSAb4dq3_Wk92ZkOc3hJpDMYwI3Uh2lvTUA0091g130_assertion
a
np:Assertion
.
dgn-np:NP233034.RAOopHSAb4dq3_Wk92ZkOc3hJpDMYwI3Uh2lvTUA0091g130_provenance
a
np:Provenance
.
dgn-np:NP233034.RAOopHSAb4dq3_Wk92ZkOc3hJpDMYwI3Uh2lvTUA0091g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP233034.RAOopHSAb4dq3_Wk92ZkOc3hJpDMYwI3Uh2lvTUA0091g130_assertion
{
miriam-gene:4036
a
ncit:C16612
.
lld:C0158945
a
ncit:C7057
.
dgn-gda:DGNf4847e1046e5bf790d1f5320f874b075
sio:SIO_000628
miriam-gene:4036
,
lld:C0158945
;
a
sio:SIO_001121
.
}
dgn-np:NP233034.RAOopHSAb4dq3_Wk92ZkOc3hJpDMYwI3Uh2lvTUA0091g130_provenance
{
dgn-np:NP233034.RAOopHSAb4dq3_Wk92ZkOc3hJpDMYwI3Uh2lvTUA0091g130_assertion
dcterms:description
"[Tests for viral DNA have proved a valid means of diagnosing congenital CMV infection in neonatal blood dried on paper (DBS) widely used in screening for metabolic and genetic diseases, as an alternative to the conventional urine culture method.]. 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:17004294
;
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:NP233034.RAOopHSAb4dq3_Wk92ZkOc3hJpDMYwI3Uh2lvTUA0091g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:10+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" .
}