@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP574488.RAB6NRAXznqM-q7uoOE6oMYKeVwjpNodCJzUZ9oETx63Q
> .
@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:NP574488.RAB6NRAXznqM-q7uoOE6oMYKeVwjpNodCJzUZ9oETx63Q130_head
{
this:
np:hasAssertion
dgn-np:NP574488.RAB6NRAXznqM-q7uoOE6oMYKeVwjpNodCJzUZ9oETx63Q130_assertion
;
np:hasProvenance
dgn-np:NP574488.RAB6NRAXznqM-q7uoOE6oMYKeVwjpNodCJzUZ9oETx63Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP574488.RAB6NRAXznqM-q7uoOE6oMYKeVwjpNodCJzUZ9oETx63Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP574488.RAB6NRAXznqM-q7uoOE6oMYKeVwjpNodCJzUZ9oETx63Q130_assertion
a
np:Assertion
.
dgn-np:NP574488.RAB6NRAXznqM-q7uoOE6oMYKeVwjpNodCJzUZ9oETx63Q130_provenance
a
np:Provenance
.
dgn-np:NP574488.RAB6NRAXznqM-q7uoOE6oMYKeVwjpNodCJzUZ9oETx63Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP574488.RAB6NRAXznqM-q7uoOE6oMYKeVwjpNodCJzUZ9oETx63Q130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN7ddbf49923e919ebe7c20af478ae527a
sio:SIO_000628
miriam-gene:4524
,
lld:C0006826
;
a
sio:SIO_001122
.
}
dgn-np:NP574488.RAB6NRAXznqM-q7uoOE6oMYKeVwjpNodCJzUZ9oETx63Q130_provenance
{
dgn-np:NP574488.RAB6NRAXznqM-q7uoOE6oMYKeVwjpNodCJzUZ9oETx63Q130_assertion
dcterms:description
"[Two common genetic variants, C677T and A1298C, of MTHFR are associated with number of human diseases, including cancer, as well as being involved in the modulation of therapy outcome to antifolate drugs.]. 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:24533714
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP574488.RAB6NRAXznqM-q7uoOE6oMYKeVwjpNodCJzUZ9oETx63Q130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:22+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" .
}