@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A
> .
@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 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:NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A130_head
{
this:
np:hasAssertion
dgn-np:NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A130_assertion
;
np:hasProvenance
dgn-np:NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A130_provenance
;
np:hasPublicationInfo
dgn-np:NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A130_assertion
a
np:Assertion
.
dgn-np:NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A130_provenance
a
np:Provenance
.
dgn-np:NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A130_assertion
{
miriam-gene:6007
a
ncit:C16612
.
lld:C0014761
a
ncit:C7057
.
dgn-gda:DGN94d176aeb768c98b7ddcaf277595c5f0
sio:SIO_000628
miriam-gene:6007
,
lld:C0014761
;
a
sio:SIO_001121
.
}
dgn-np:NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A130_provenance
{
dgn-np:NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A130_assertion
dct: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: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:NP365007.RAB4Kmv_sV8RM-YcDUWBMMMT2OVgT18n1EPoMFe9dhv2A130_publicationInfo
{
this:
dct:created
"2014-10-02T12:35:33+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}