@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync
> .
@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:NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync130_head
{
this:
np:hasAssertion
dgn-np:NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync130_assertion
;
np:hasProvenance
dgn-np:NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync130_provenance
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np:hasPublicationInfo
dgn-np:NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync130_assertion
a
np:Assertion
.
dgn-np:NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync130_provenance
a
np:Provenance
.
dgn-np:NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGNbae60f37fcbc3be98d6b7169fd611fb6
sio:SIO_000628
miriam-gene:4524
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync130_provenance
{
dgn-np:NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync130_assertion
dcterms:description
"[Encouraged by recent studies on the MTHFR 677C>T polymorphism and breast cancer risk that suggested an association of the 677 TT genotype with increased breast cancer susceptibility in premenopausal women, we performed an analysis of the relationship between breast cancer risk and the MTHFR 677C>T polymorphism in 210 premenopausal breast cancer patients and sex- and agematched healthy control subjects.]. 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:17453338
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP61428.RAnuEc_DSDwH_XXyhJqLNERDWG4LWulRg5Gg1bKjUnync130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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
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dgn-void:disgenetrdf
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"v2.1.0" .
}