@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg
> .
@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:NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg130_head
{
this:
np:hasAssertion
dgn-np:NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg130_assertion
;
np:hasProvenance
dgn-np:NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg130_provenance
;
np:hasPublicationInfo
dgn-np:NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg130_assertion
a
np:Assertion
.
dgn-np:NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg130_provenance
a
np:Provenance
.
dgn-np:NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg130_assertion
{
miriam-gene:6007
a
ncit:C16612
.
lld:C0158962
a
ncit:C7057
.
dgn-gda:DGNd07bb7d55e869fa2f0529a66fcc3f9cf
sio:SIO_000628
miriam-gene:6007
,
lld:C0158962
;
a
sio:SIO_001122
.
}
dgn-np:NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg130_provenance
{
dgn-np:NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg130_assertion
dcterms:description
"[Use of the polymerase chain reaction (PCR) for detection of the RHD gene can measure the RHD gene status for unborn babies at risk for hemolytic disease of the newborn (HDN).]. 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:11288127
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP61935.RAQz_wAF7uf2NNvaqmt3MEweXZKb1D9fMpUKo0OV0lkCg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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" .
}