@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU
> .
@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:NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU130_head
{
this:
np:hasAssertion
dgn-np:NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU130_assertion
;
np:hasProvenance
dgn-np:NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU130_provenance
;
np:hasPublicationInfo
dgn-np:NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU130_assertion
a
np:Assertion
.
dgn-np:NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU130_provenance
a
np:Provenance
.
dgn-np:NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU130_assertion
{
miriam-gene:4163
a
ncit:C16612
.
lld:C0007129
a
ncit:C7057
.
dgn-gda:DGN9add371cdf368b064d87a5eb4c340687
sio:SIO_000628
miriam-gene:4163
,
lld:C0007129
;
a
sio:SIO_001121
.
}
dgn-np:NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU130_provenance
{
dgn-np:NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU130_assertion
dcterms:description
"[We aimed to (a) highlight the risk of maternal cell contamination (MCC) in biochemical prenatal diagnosis, (b) establish the threshold of these biochemical assays to MCC, and (c) document the sensitivity of PCR based genotyping of microsatellites for the detection of MCC in prenatal diagnosis of inborn errors by biochemical analysis.]. 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:15635073
;
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:NP851639.RAeYMey7KUCmkUyULIlU3BV2aV-KPwfZHP5sxar7bw6iU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:40+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" .
}