@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP266182.RAxVPsbzgqxwmiKSS91wukdKVpVnHT4fJF1ickj98higA
> .
@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:NP266182.RAxVPsbzgqxwmiKSS91wukdKVpVnHT4fJF1ickj98higA130_head
{
this:
np:hasAssertion
dgn-np:NP266182.RAxVPsbzgqxwmiKSS91wukdKVpVnHT4fJF1ickj98higA130_assertion
;
np:hasProvenance
dgn-np:NP266182.RAxVPsbzgqxwmiKSS91wukdKVpVnHT4fJF1ickj98higA130_provenance
;
np:hasPublicationInfo
dgn-np:NP266182.RAxVPsbzgqxwmiKSS91wukdKVpVnHT4fJF1ickj98higA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP266182.RAxVPsbzgqxwmiKSS91wukdKVpVnHT4fJF1ickj98higA130_assertion
a
np:Assertion
.
dgn-np:NP266182.RAxVPsbzgqxwmiKSS91wukdKVpVnHT4fJF1ickj98higA130_provenance
a
np:Provenance
.
dgn-np:NP266182.RAxVPsbzgqxwmiKSS91wukdKVpVnHT4fJF1ickj98higA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP266182.RAxVPsbzgqxwmiKSS91wukdKVpVnHT4fJF1ickj98higA130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0278987
a
ncit:C7057
.
dgn-gda:DGN31bfc0b39b4eae7e29a9ca31c6c2eaf1
sio:SIO_000628
miriam-gene:4524
,
lld:C0278987
;
a
sio:SIO_001121
.
}
dgn-np:NP266182.RAxVPsbzgqxwmiKSS91wukdKVpVnHT4fJF1ickj98higA130_provenance
{
dgn-np:NP266182.RAxVPsbzgqxwmiKSS91wukdKVpVnHT4fJF1ickj98higA130_assertion
dcterms:description
"[In the present study, we have examined the SNP of methylenetetrahydrofolate reductase (MTHFR) C677T, which affects DNA methylation patterns and is linked to elevated plasma homocysteine levels in 208 patients with gemcitabine/cisplatin-treated stage IV non-small-cell lung cancer (NSCLC).]. 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:15217535
;
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:NP266182.RAxVPsbzgqxwmiKSS91wukdKVpVnHT4fJF1ickj98higA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:28+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" .
}