@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs
> .
@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:NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_head
{
this:
np:hasAssertion
dgn-np:NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_assertion
;
np:hasProvenance
dgn-np:NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_provenance
;
np:hasPublicationInfo
dgn-np:NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_assertion
a
np:Assertion
.
dgn-np:NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_provenance
a
np:Provenance
.
dgn-np:NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_assertion
{
miriam-gene:6470
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGNbaa8211b6a512a4bda2638bed9f3ae20
sio:SIO_000628
miriam-gene:6470
,
lld:C0014544
;
a
sio:SIO_001122
.
}
dgn-np:NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_provenance
{
dgn-np:NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_assertion
dcterms:description
"[To investigate this further, a new cohort of women with epilepsy has been identified from maternity hospital records and genotyped for polymorphisms in MTHFR, serine hydroxymethyl transferase (SHMT1), methionine synthase (MTR) and methionine synthase reductase (MTRR).]. 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:17904392
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP93042.RAUU4_pW8AJwzQe9W6aYIFz5YO4043sLMV8eV__SlXHKs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:46+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" .
}