@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP823903.RAnYlrKkXgHIci610n-CrQX3UGXle6G3RJgKJq2S3Ruxc
> .
@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:NP823903.RAnYlrKkXgHIci610n-CrQX3UGXle6G3RJgKJq2S3Ruxc130_head
{
this:
np:hasAssertion
dgn-np:NP823903.RAnYlrKkXgHIci610n-CrQX3UGXle6G3RJgKJq2S3Ruxc130_assertion
;
np:hasProvenance
dgn-np:NP823903.RAnYlrKkXgHIci610n-CrQX3UGXle6G3RJgKJq2S3Ruxc130_provenance
;
np:hasPublicationInfo
dgn-np:NP823903.RAnYlrKkXgHIci610n-CrQX3UGXle6G3RJgKJq2S3Ruxc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP823903.RAnYlrKkXgHIci610n-CrQX3UGXle6G3RJgKJq2S3Ruxc130_assertion
a
np:Assertion
.
dgn-np:NP823903.RAnYlrKkXgHIci610n-CrQX3UGXle6G3RJgKJq2S3Ruxc130_provenance
a
np:Provenance
.
dgn-np:NP823903.RAnYlrKkXgHIci610n-CrQX3UGXle6G3RJgKJq2S3Ruxc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP823903.RAnYlrKkXgHIci610n-CrQX3UGXle6G3RJgKJq2S3Ruxc130_assertion
{
miriam-gene:1791
a
ncit:C16612
.
lld:C0080178
a
ncit:C7057
.
dgn-gda:DGN02ffee81cdfff2dec0774886b25e544b
sio:SIO_000628
miriam-gene:1791
,
lld:C0080178
;
a
sio:SIO_001121
.
}
dgn-np:NP823903.RAnYlrKkXgHIci610n-CrQX3UGXle6G3RJgKJq2S3Ruxc130_provenance
{
dgn-np:NP823903.RAnYlrKkXgHIci610n-CrQX3UGXle6G3RJgKJq2S3Ruxc130_assertion
dcterms:description
"[The association between the risk of spina bifida and both the maternal and embryonic genotype for the NOS3 G894T variant was evaluated in data from 301 families by using the transmission disequilibrium test (TDT) and log-linear modeling.]. 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:15039923
;
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:NP823903.RAnYlrKkXgHIci610n-CrQX3UGXle6G3RJgKJq2S3Ruxc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:24+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: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" .
}