@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP709956.RA68OFBbNTSUe45I46ks-YwMN3NTsmjkrmJ5irdjSr600
> .
@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:NP709956.RA68OFBbNTSUe45I46ks-YwMN3NTsmjkrmJ5irdjSr600130_head
{
this:
np:hasAssertion
dgn-np:NP709956.RA68OFBbNTSUe45I46ks-YwMN3NTsmjkrmJ5irdjSr600130_assertion
;
np:hasProvenance
dgn-np:NP709956.RA68OFBbNTSUe45I46ks-YwMN3NTsmjkrmJ5irdjSr600130_provenance
;
np:hasPublicationInfo
dgn-np:NP709956.RA68OFBbNTSUe45I46ks-YwMN3NTsmjkrmJ5irdjSr600130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP709956.RA68OFBbNTSUe45I46ks-YwMN3NTsmjkrmJ5irdjSr600130_assertion
a
np:Assertion
.
dgn-np:NP709956.RA68OFBbNTSUe45I46ks-YwMN3NTsmjkrmJ5irdjSr600130_provenance
a
np:Provenance
.
dgn-np:NP709956.RA68OFBbNTSUe45I46ks-YwMN3NTsmjkrmJ5irdjSr600130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP709956.RA68OFBbNTSUe45I46ks-YwMN3NTsmjkrmJ5irdjSr600130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0151945
a
ncit:C7057
.
dgn-gda:DGNf9c109c438e500df7a83f52a706d1718
sio:SIO_000628
miriam-gene:4524
,
lld:C0151945
;
a
sio:SIO_001121
.
}
dgn-np:NP709956.RA68OFBbNTSUe45I46ks-YwMN3NTsmjkrmJ5irdjSr600130_provenance
{
dgn-np:NP709956.RA68OFBbNTSUe45I46ks-YwMN3NTsmjkrmJ5irdjSr600130_assertion
dcterms:description
"[We report three patients with cerebral vein thrombosis (CVT) in which the only risk factor we were able to identify was increased blood homocysteine levels and the C677T polymorphism in both alleles of the methylene tetrahydrofolate reductase MTHFR gene.]. 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:12522678
;
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:NP709956.RA68OFBbNTSUe45I46ks-YwMN3NTsmjkrmJ5irdjSr600130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:11+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" .
}