@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg
> .
@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:NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg130_head
{
this:
np:hasAssertion
dgn-np:NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg130_assertion
;
np:hasProvenance
dgn-np:NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg130_provenance
;
np:hasPublicationInfo
dgn-np:NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg130_assertion
a
np:Assertion
.
dgn-np:NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg130_provenance
a
np:Provenance
.
dgn-np:NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg130_assertion
{
miriam-gene:4548
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN9434acaea1126724a70ddfe657bd0dc0
sio:SIO_000628
miriam-gene:4548
,
lld:C0376358
;
a
sio:SIO_001121
.
}
dgn-np:NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg130_provenance
{
dgn-np:NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg130_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
;
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:NP273663.RAmT0uGs8khKyRRU21r2ElMJb0qII9eR1W0NwRmiwInhg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:34+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" .
}