@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP578639.RAyNM7Xvj09CbVacS2qOpRzNm7k9EFbpB1oAyEMBohjY0
> .
@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:NP578639.RAyNM7Xvj09CbVacS2qOpRzNm7k9EFbpB1oAyEMBohjY0130_head
{
this:
np:hasAssertion
dgn-np:NP578639.RAyNM7Xvj09CbVacS2qOpRzNm7k9EFbpB1oAyEMBohjY0130_assertion
;
np:hasProvenance
dgn-np:NP578639.RAyNM7Xvj09CbVacS2qOpRzNm7k9EFbpB1oAyEMBohjY0130_provenance
;
np:hasPublicationInfo
dgn-np:NP578639.RAyNM7Xvj09CbVacS2qOpRzNm7k9EFbpB1oAyEMBohjY0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP578639.RAyNM7Xvj09CbVacS2qOpRzNm7k9EFbpB1oAyEMBohjY0130_assertion
a
np:Assertion
.
dgn-np:NP578639.RAyNM7Xvj09CbVacS2qOpRzNm7k9EFbpB1oAyEMBohjY0130_provenance
a
np:Provenance
.
dgn-np:NP578639.RAyNM7Xvj09CbVacS2qOpRzNm7k9EFbpB1oAyEMBohjY0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP578639.RAyNM7Xvj09CbVacS2qOpRzNm7k9EFbpB1oAyEMBohjY0130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0206708
a
ncit:C7057
.
dgn-gda:DGNbb7000fe9c02d44f6f0186aaf734f2e8
sio:SIO_000628
miriam-gene:4524
,
lld:C0206708
;
a
sio:SIO_001121
.
}
dgn-np:NP578639.RAyNM7Xvj09CbVacS2qOpRzNm7k9EFbpB1oAyEMBohjY0130_provenance
{
dgn-np:NP578639.RAyNM7Xvj09CbVacS2qOpRzNm7k9EFbpB1oAyEMBohjY0130_assertion
dcterms:description
"[Serum folate concentration is inversely associated with the risk of cervical cancer, and the MTHFR variant genotype may increase CIN and cervical cancer risk in women with low folate or vitamin B12 status.]. 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:21052817
;
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:NP578639.RAyNM7Xvj09CbVacS2qOpRzNm7k9EFbpB1oAyEMBohjY0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:48+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" .
}