@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP816184.RAFyklGsFDImsTdPIrAZio9dtzJTHxOkvHy5KBMJGDcfk
> .
@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:NP816184.RAFyklGsFDImsTdPIrAZio9dtzJTHxOkvHy5KBMJGDcfk130_head
{
this:
np:hasAssertion
dgn-np:NP816184.RAFyklGsFDImsTdPIrAZio9dtzJTHxOkvHy5KBMJGDcfk130_assertion
;
np:hasProvenance
dgn-np:NP816184.RAFyklGsFDImsTdPIrAZio9dtzJTHxOkvHy5KBMJGDcfk130_provenance
;
np:hasPublicationInfo
dgn-np:NP816184.RAFyklGsFDImsTdPIrAZio9dtzJTHxOkvHy5KBMJGDcfk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP816184.RAFyklGsFDImsTdPIrAZio9dtzJTHxOkvHy5KBMJGDcfk130_assertion
a
np:Assertion
.
dgn-np:NP816184.RAFyklGsFDImsTdPIrAZio9dtzJTHxOkvHy5KBMJGDcfk130_provenance
a
np:Provenance
.
dgn-np:NP816184.RAFyklGsFDImsTdPIrAZio9dtzJTHxOkvHy5KBMJGDcfk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP816184.RAFyklGsFDImsTdPIrAZio9dtzJTHxOkvHy5KBMJGDcfk130_assertion
{
miriam-gene:875
a
ncit:C16612
.
lld:C1168401
a
ncit:C7057
.
dgn-gda:DGN1240ff416a5ef74356eb1d720f6453e2
sio:SIO_000628
miriam-gene:875
,
lld:C1168401
;
a
sio:SIO_001121
.
}
dgn-np:NP816184.RAFyklGsFDImsTdPIrAZio9dtzJTHxOkvHy5KBMJGDcfk130_provenance
{
dgn-np:NP816184.RAFyklGsFDImsTdPIrAZio9dtzJTHxOkvHy5KBMJGDcfk130_assertion
dcterms:description
"[We conducted a case-control study (265 HNSCC cases and 466 non-cancer controls) to investigate associations of MTHFR C677T and A1298C, MTR A2756G, MTRR A66G, RFC1 A80G, MTHFD1 G1958A, CBS 844ins68, TC2 C776G and A67G, SHMT C1420T and BHMT G742A polymorphisms with HNSCC risk.]. 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:22051736
;
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:NP816184.RAFyklGsFDImsTdPIrAZio9dtzJTHxOkvHy5KBMJGDcfk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:20+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" .
}