@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg
> .
@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:NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg130_head
{
this:
np:hasAssertion
dgn-np:NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg130_assertion
;
np:hasProvenance
dgn-np:NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg130_provenance
;
np:hasPublicationInfo
dgn-np:NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg130_assertion
a
np:Assertion
.
dgn-np:NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg130_provenance
a
np:Provenance
.
dgn-np:NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg130_assertion
{
miriam-gene:5981
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN3bf9e78f1f3cf16a9a621e957084268c
sio:SIO_000628
miriam-gene:5981
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg130_provenance
{
dgn-np:NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg130_assertion
dcterms:description
"[Conversely, for women over 50, the risk of breast cancer development was statistically associated with the MTHFR 677CT genotype, but especially significant was risk associated with the presence of the polymorphic allele of cSHMT C1420T (P = 0.0120) and the protective effect associated with the RFC1 G80A polymorphism allele (P = 0.0021), was restrict to this age group.]. 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:22134752
;
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:NP809891.RALQRcjpmm3m1f0mCSH9AMzREmiszk1VmwGHk_nT9VaHg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:16+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" .
}