@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg130_head
{
this:
np:hasAssertion
dgn-np:NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg130_assertion
;
np:hasProvenance
dgn-np:NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg130_provenance
;
np:hasPublicationInfo
dgn-np:NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg130_assertion
a
np:Assertion
.
dgn-np:NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg130_provenance
a
np:Provenance
.
dgn-np:NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0025284
a
ncit:C7057
.
dgn-gda:DGNf1a431e6852f2ad50573062a0826dba0
sio:SIO_000628
miriam-gene:4524
,
lld:C0025284
;
a
sio:SIO_001122
.
}
dgn-np:NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg130_provenance
{
dgn-np:NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg130_assertion
dcterms:description
"[In spite of the established effect of the MTHFR 677 TT genotype on DNA hypomethylation with concomitant inadequate folate levels, the MTHFR 677 TT genotype is not associated with individual susceptibility to HGG.]. 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:16821630
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP91534.RASlKHWqjADBUloaIofeWQqAWG7Nwlu6O3BE-DbBdQieg130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:30+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}