@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP310372.RAtYu5SMpQ1uxjl7igOf5c9nbhHOHYDhYQ7vR1t9qDoks
> .
@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:NP310372.RAtYu5SMpQ1uxjl7igOf5c9nbhHOHYDhYQ7vR1t9qDoks130_head
{
this:
np:hasAssertion
dgn-np:NP310372.RAtYu5SMpQ1uxjl7igOf5c9nbhHOHYDhYQ7vR1t9qDoks130_assertion
;
np:hasProvenance
dgn-np:NP310372.RAtYu5SMpQ1uxjl7igOf5c9nbhHOHYDhYQ7vR1t9qDoks130_provenance
;
np:hasPublicationInfo
dgn-np:NP310372.RAtYu5SMpQ1uxjl7igOf5c9nbhHOHYDhYQ7vR1t9qDoks130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP310372.RAtYu5SMpQ1uxjl7igOf5c9nbhHOHYDhYQ7vR1t9qDoks130_assertion
a
np:Assertion
.
dgn-np:NP310372.RAtYu5SMpQ1uxjl7igOf5c9nbhHOHYDhYQ7vR1t9qDoks130_provenance
a
np:Provenance
.
dgn-np:NP310372.RAtYu5SMpQ1uxjl7igOf5c9nbhHOHYDhYQ7vR1t9qDoks130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP310372.RAtYu5SMpQ1uxjl7igOf5c9nbhHOHYDhYQ7vR1t9qDoks130_assertion
{
miriam-gene:4522
a
ncit:C16612
.
lld:C0278996
a
ncit:C7057
.
dgn-gda:DGNe6532cfc259bff9de95b1db576080494
sio:SIO_000628
miriam-gene:4522
,
lld:C0278996
;
a
sio:SIO_001121
.
}
dgn-np:NP310372.RAtYu5SMpQ1uxjl7igOf5c9nbhHOHYDhYQ7vR1t9qDoks130_provenance
{
dgn-np:NP310372.RAtYu5SMpQ1uxjl7igOf5c9nbhHOHYDhYQ7vR1t9qDoks130_assertion
dcterms:description
"[The objectives were to investigate MTHFD1 G1958A, BHMT G742A, TC2 C776G and TC2 A67G polymorphisms involved in folate metabolism on head and neck cancer risk and the association between these polymorphisms with risk factors.]. 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:21630102
;
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:NP310372.RAtYu5SMpQ1uxjl7igOf5c9nbhHOHYDhYQ7vR1t9qDoks130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:58+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" .
}