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http://rdf.disgenet.org/nanopublications.trig#NP451379.RAFanix-2_M-ew4bMnpMyGFb--cA-wyhz79-TJt0XDcLY
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
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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/
> .
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http://identifiers.org/pubmed/
> .
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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#
> .
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{
this:
np:hasAssertion
dgn-np:NP451379.RAFanix-2_M-ew4bMnpMyGFb--cA-wyhz79-TJt0XDcLY130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
.
dgn-np:NP451379.RAFanix-2_M-ew4bMnpMyGFb--cA-wyhz79-TJt0XDcLY130_assertion
a
np:Assertion
.
dgn-np:NP451379.RAFanix-2_M-ew4bMnpMyGFb--cA-wyhz79-TJt0XDcLY130_provenance
a
np:Provenance
.
dgn-np:NP451379.RAFanix-2_M-ew4bMnpMyGFb--cA-wyhz79-TJt0XDcLY130_publicationInfo
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{
miriam-gene:4552
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN97f64a470667c1ff32d30cd617c400d2
sio:SIO_000628
miriam-gene:4552
,
lld:C0376358
;
a
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.
}
dgn-np:NP451379.RAFanix-2_M-ew4bMnpMyGFb--cA-wyhz79-TJt0XDcLY130_provenance
{
dgn-np:NP451379.RAFanix-2_M-ew4bMnpMyGFb--cA-wyhz79-TJt0XDcLY130_assertion
dcterms:description
"[The single nucleotide polymorphisms, MTHFR C677T, A1298C, MTR A2756G and MTRR A66G, cause alteration in the homocysteine levels and reduced enzymatic activity that generates deficiency in the assimilation of folates associated with DNA damage; that is, why it is important to know if the single nucleotide polymorphisms are associated with the pathological characteristics and development of prostate cancer, through a case-control retrospective study.]. 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:23459165
;
prov:wasDerivedFrom
dgn-void:befree-20140225
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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 .
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dgn-np:NP451379.RAFanix-2_M-ew4bMnpMyGFb--cA-wyhz79-TJt0XDcLY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:29+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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> , <
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> ;
pav:createdBy
<
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