@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es
> .
@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:NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es130_head
{
this:
np:hasAssertion
dgn-np:NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es130_assertion
;
np:hasProvenance
dgn-np:NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es130_provenance
;
np:hasPublicationInfo
dgn-np:NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es130_assertion
a
np:Assertion
.
dgn-np:NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es130_provenance
a
np:Provenance
.
dgn-np:NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C1458155
a
ncit:C7057
.
dgn-gda:DGN0bc9a3acded6075043e1e9a72769e1a7
sio:SIO_000628
miriam-gene:4524
,
lld:C1458155
;
a
sio:SIO_001121
.
}
dgn-np:NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es130_provenance
{
dgn-np:NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es130_assertion
dcterms:description
"[To evaluate the C677T and A1298C functional polymorphisms in the MTHFR gene and their associations with breast cancer risk, as well as the potential modifying effect by plasma folate status on the MTHFR-associated risk, a hospital-based case-control study was conducted on a Taiwanese population consisting of 146 histologically confirmed incident breast cancer cases and their 285 age-matched controls without a history of cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:16777985
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP23365.RASdUfGp-GYzF_9HgfXaIe315bfsTAnJlhJlkFWKhM3Es130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:09+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" .
}