@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP80376.RAQ2NQXCgYa25TFmFSjmmfh6m-LvsSBOjQMB_kB8gJxp8
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP80376.RAQ2NQXCgYa25TFmFSjmmfh6m-LvsSBOjQMB_kB8gJxp8130_head
{
this:
np:hasAssertion
dgn-np:NP80376.RAQ2NQXCgYa25TFmFSjmmfh6m-LvsSBOjQMB_kB8gJxp8130_assertion
;
np:hasProvenance
dgn-np:NP80376.RAQ2NQXCgYa25TFmFSjmmfh6m-LvsSBOjQMB_kB8gJxp8130_provenance
;
np:hasPublicationInfo
dgn-np:NP80376.RAQ2NQXCgYa25TFmFSjmmfh6m-LvsSBOjQMB_kB8gJxp8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP80376.RAQ2NQXCgYa25TFmFSjmmfh6m-LvsSBOjQMB_kB8gJxp8130_assertion
a
np:Assertion
.
dgn-np:NP80376.RAQ2NQXCgYa25TFmFSjmmfh6m-LvsSBOjQMB_kB8gJxp8130_provenance
a
np:Provenance
.
dgn-np:NP80376.RAQ2NQXCgYa25TFmFSjmmfh6m-LvsSBOjQMB_kB8gJxp8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP80376.RAQ2NQXCgYa25TFmFSjmmfh6m-LvsSBOjQMB_kB8gJxp8130_assertion
{
miriam-gene:7298
a
ncit:C16612
.
lld:C0027794
a
ncit:C7057
.
dgn-gda:DGN89b184ab2ff2485e27621ed727294c1b
sio:SIO_000628
miriam-gene:7298
,
lld:C0027794
;
a
sio:SIO_001122
.
}
dgn-np:NP80376.RAQ2NQXCgYa25TFmFSjmmfh6m-LvsSBOjQMB_kB8gJxp8130_provenance
{
dgn-np:NP80376.RAQ2NQXCgYa25TFmFSjmmfh6m-LvsSBOjQMB_kB8gJxp8130_assertion
dcterms:description
"[ TYMS polymorphism appears to be not universally associated with NTD risk across Caucasian samples. The elevated risk of spina bifida in U.S. samples appears to be driven by an unusually low risk allele (2x 28 bp) frequency in control samples. Family base]. 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:15259039
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP80376.RAQ2NQXCgYa25TFmFSjmmfh6m-LvsSBOjQMB_kB8gJxp8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:24+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}