@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP526471.RAsbGdqeiKYg9K7cLjxK5mbl1z3do8GBWILHoe76XC_sY
> .
@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:NP526471.RAsbGdqeiKYg9K7cLjxK5mbl1z3do8GBWILHoe76XC_sY130_head
{
this:
np:hasAssertion
dgn-np:NP526471.RAsbGdqeiKYg9K7cLjxK5mbl1z3do8GBWILHoe76XC_sY130_assertion
;
np:hasProvenance
dgn-np:NP526471.RAsbGdqeiKYg9K7cLjxK5mbl1z3do8GBWILHoe76XC_sY130_provenance
;
np:hasPublicationInfo
dgn-np:NP526471.RAsbGdqeiKYg9K7cLjxK5mbl1z3do8GBWILHoe76XC_sY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP526471.RAsbGdqeiKYg9K7cLjxK5mbl1z3do8GBWILHoe76XC_sY130_assertion
a
np:Assertion
.
dgn-np:NP526471.RAsbGdqeiKYg9K7cLjxK5mbl1z3do8GBWILHoe76XC_sY130_provenance
a
np:Provenance
.
dgn-np:NP526471.RAsbGdqeiKYg9K7cLjxK5mbl1z3do8GBWILHoe76XC_sY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP526471.RAsbGdqeiKYg9K7cLjxK5mbl1z3do8GBWILHoe76XC_sY130_assertion
{
miriam-gene:4552
a
ncit:C16612
.
lld:C0013080
a
ncit:C7057
.
dgn-gda:DGN14661ade25ff0004b00b24d996cca9df
sio:SIO_000628
miriam-gene:4552
,
lld:C0013080
;
a
sio:SIO_001121
.
}
dgn-np:NP526471.RAsbGdqeiKYg9K7cLjxK5mbl1z3do8GBWILHoe76XC_sY130_provenance
{
dgn-np:NP526471.RAsbGdqeiKYg9K7cLjxK5mbl1z3do8GBWILHoe76XC_sY130_assertion
dcterms:description
"[At the same time, micronucleus data indicate that the MTRR 66GG variant may represent another individual trait of relative genomic instability, thus supporting epidemiological data on increased risk of Down syndrome conception in MTRR 66GG subjects.]. 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:12807760
;
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:NP526471.RAsbGdqeiKYg9K7cLjxK5mbl1z3do8GBWILHoe76XC_sY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:15+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" .
}