@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP630059.RAmvWgrh2Eb5dCXB7lbmArSs7vexaugyF53VSk1551Fvw
> .
@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:NP630059.RAmvWgrh2Eb5dCXB7lbmArSs7vexaugyF53VSk1551Fvw130_head
{
this:
np:hasAssertion
dgn-np:NP630059.RAmvWgrh2Eb5dCXB7lbmArSs7vexaugyF53VSk1551Fvw130_assertion
;
np:hasProvenance
dgn-np:NP630059.RAmvWgrh2Eb5dCXB7lbmArSs7vexaugyF53VSk1551Fvw130_provenance
;
np:hasPublicationInfo
dgn-np:NP630059.RAmvWgrh2Eb5dCXB7lbmArSs7vexaugyF53VSk1551Fvw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP630059.RAmvWgrh2Eb5dCXB7lbmArSs7vexaugyF53VSk1551Fvw130_assertion
a
np:Assertion
.
dgn-np:NP630059.RAmvWgrh2Eb5dCXB7lbmArSs7vexaugyF53VSk1551Fvw130_provenance
a
np:Provenance
.
dgn-np:NP630059.RAmvWgrh2Eb5dCXB7lbmArSs7vexaugyF53VSk1551Fvw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP630059.RAmvWgrh2Eb5dCXB7lbmArSs7vexaugyF53VSk1551Fvw130_assertion
{
miriam-gene:23743
a
ncit:C16612
.
lld:C0007570
a
ncit:C7057
.
dgn-gda:DGNd5299583aae9176a9a6ea561db5acd11
sio:SIO_000628
miriam-gene:23743
,
lld:C0007570
;
a
sio:SIO_001121
.
}
dgn-np:NP630059.RAmvWgrh2Eb5dCXB7lbmArSs7vexaugyF53VSk1551Fvw130_provenance
{
dgn-np:NP630059.RAmvWgrh2Eb5dCXB7lbmArSs7vexaugyF53VSk1551Fvw130_assertion
dcterms:description
"[A set of 10 gene polymorphisms (MTHFR rs1801133, MTR rs1805087, MTHFD1 rs2236225, MTRR rs1801394, CBS 844ins68, BHMT1 rs7356530 and rs3733890, BHMT2 rs526264 and rs625879, and TCN2 rs1801198) was tested in 134 patients with CD and 160 matched healthy controls.]. 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:21688148
;
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:NP630059.RAmvWgrh2Eb5dCXB7lbmArSs7vexaugyF53VSk1551Fvw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:20+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" .
}