@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP424124.RA3X_eaF4ygkGxN2P7tYQ32nLudXygsG7nLSLdZc7rUr0
> .
@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:NP424124.RA3X_eaF4ygkGxN2P7tYQ32nLudXygsG7nLSLdZc7rUr0130_head
{
this:
np:hasAssertion
dgn-np:NP424124.RA3X_eaF4ygkGxN2P7tYQ32nLudXygsG7nLSLdZc7rUr0130_assertion
;
np:hasProvenance
dgn-np:NP424124.RA3X_eaF4ygkGxN2P7tYQ32nLudXygsG7nLSLdZc7rUr0130_provenance
;
np:hasPublicationInfo
dgn-np:NP424124.RA3X_eaF4ygkGxN2P7tYQ32nLudXygsG7nLSLdZc7rUr0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP424124.RA3X_eaF4ygkGxN2P7tYQ32nLudXygsG7nLSLdZc7rUr0130_assertion
a
np:Assertion
.
dgn-np:NP424124.RA3X_eaF4ygkGxN2P7tYQ32nLudXygsG7nLSLdZc7rUr0130_provenance
a
np:Provenance
.
dgn-np:NP424124.RA3X_eaF4ygkGxN2P7tYQ32nLudXygsG7nLSLdZc7rUr0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP424124.RA3X_eaF4ygkGxN2P7tYQ32nLudXygsG7nLSLdZc7rUr0130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0747845
a
ncit:C7057
.
dgn-gda:DGN8904240641beb854dc951169372727ce
sio:SIO_000628
miriam-gene:4524
,
lld:C0747845
;
a
sio:SIO_001121
.
}
dgn-np:NP424124.RA3X_eaF4ygkGxN2P7tYQ32nLudXygsG7nLSLdZc7rUr0130_provenance
{
dgn-np:NP424124.RA3X_eaF4ygkGxN2P7tYQ32nLudXygsG7nLSLdZc7rUr0130_assertion
dcterms:description
"[The methylenetetrahydrofolate reductase (MTHFR) gene C677T and A1298C polymorphisms are commonly associated with defects in folate dependent homocysteine metabolism and have been implicated as risk factors for recurrent embryo loss in early pregnancy.]. 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:11938441
;
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:NP424124.RA3X_eaF4ygkGxN2P7tYQ32nLudXygsG7nLSLdZc7rUr0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:11+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" .
}