@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP457106.RAQ19kkCDM4UyK8688bVZPKKQU7zpfLHSE3kC8f9Qq1uM
> .
@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:NP457106.RAQ19kkCDM4UyK8688bVZPKKQU7zpfLHSE3kC8f9Qq1uM130_head
{
this:
np:hasAssertion
dgn-np:NP457106.RAQ19kkCDM4UyK8688bVZPKKQU7zpfLHSE3kC8f9Qq1uM130_assertion
;
np:hasProvenance
dgn-np:NP457106.RAQ19kkCDM4UyK8688bVZPKKQU7zpfLHSE3kC8f9Qq1uM130_provenance
;
np:hasPublicationInfo
dgn-np:NP457106.RAQ19kkCDM4UyK8688bVZPKKQU7zpfLHSE3kC8f9Qq1uM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP457106.RAQ19kkCDM4UyK8688bVZPKKQU7zpfLHSE3kC8f9Qq1uM130_assertion
a
np:Assertion
.
dgn-np:NP457106.RAQ19kkCDM4UyK8688bVZPKKQU7zpfLHSE3kC8f9Qq1uM130_provenance
a
np:Provenance
.
dgn-np:NP457106.RAQ19kkCDM4UyK8688bVZPKKQU7zpfLHSE3kC8f9Qq1uM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP457106.RAQ19kkCDM4UyK8688bVZPKKQU7zpfLHSE3kC8f9Qq1uM130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0024314
a
ncit:C7057
.
dgn-gda:DGN9c71b35b9430efcf8d599c59c7e101e6
sio:SIO_000628
miriam-gene:4524
,
lld:C0024314
;
a
sio:SIO_001121
.
}
dgn-np:NP457106.RAQ19kkCDM4UyK8688bVZPKKQU7zpfLHSE3kC8f9Qq1uM130_provenance
{
dgn-np:NP457106.RAQ19kkCDM4UyK8688bVZPKKQU7zpfLHSE3kC8f9Qq1uM130_assertion
dcterms:description
"[Because folate is the cornerstone in DNA synthesis, we analysed herein if the polymorphisms in MTHFR gene can alter the susceptibility of lymphoproliferative disease risk and if it has an effect on chemotherapy response.]. 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:16944145
;
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:NP457106.RAQ19kkCDM4UyK8688bVZPKKQU7zpfLHSE3kC8f9Qq1uM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:32+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" .
}