@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI
> .
@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:NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI130_head
{
this:
np:hasAssertion
dgn-np:NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI130_assertion
;
np:hasProvenance
dgn-np:NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI130_provenance
;
np:hasPublicationInfo
dgn-np:NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI130_assertion
a
np:Assertion
.
dgn-np:NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI130_provenance
a
np:Provenance
.
dgn-np:NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGNddabf409515e41f86a693fd3e9810e69
sio:SIO_000628
miriam-gene:4524
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI130_provenance
{
dgn-np:NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI130_assertion
dcterms:description
"[This study points out the importance of the interactions between the MTHFR C677T, MTHFR A1298C and MTR A2756G polymorphisms, and also highlights the relevance of the MTR A2756G polymorphism and age in breast cancer risk.]. 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:23155246
;
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:NP231372.RAMZiLdNjUWrNZA1vs1UoBTCTgnHt9MU_gXescVkhiXUI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:09+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" .
}