@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP511982.RAV8BbcHhwd2MI_Pe9f-HCjQPAkwhZTHXzJpWVzl0Mthw
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP511982.RAV8BbcHhwd2MI_Pe9f-HCjQPAkwhZTHXzJpWVzl0Mthw130_assertion
;
np:hasProvenance
dgn-np:NP511982.RAV8BbcHhwd2MI_Pe9f-HCjQPAkwhZTHXzJpWVzl0Mthw130_provenance
;
np:hasPublicationInfo
dgn-np:NP511982.RAV8BbcHhwd2MI_Pe9f-HCjQPAkwhZTHXzJpWVzl0Mthw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP511982.RAV8BbcHhwd2MI_Pe9f-HCjQPAkwhZTHXzJpWVzl0Mthw130_assertion
a
np:Assertion
.
dgn-np:NP511982.RAV8BbcHhwd2MI_Pe9f-HCjQPAkwhZTHXzJpWVzl0Mthw130_provenance
a
np:Provenance
.
dgn-np:NP511982.RAV8BbcHhwd2MI_Pe9f-HCjQPAkwhZTHXzJpWVzl0Mthw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP511982.RAV8BbcHhwd2MI_Pe9f-HCjQPAkwhZTHXzJpWVzl0Mthw130_assertion
{
miriam-gene:3373
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNd388fd5b658150086e65a487bb5ce32e
sio:SIO_000628
miriam-gene:3373
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP511982.RAV8BbcHhwd2MI_Pe9f-HCjQPAkwhZTHXzJpWVzl0Mthw130_provenance
{
dgn-np:NP511982.RAV8BbcHhwd2MI_Pe9f-HCjQPAkwhZTHXzJpWVzl0Mthw130_assertion
dcterms:description
"[Since nasopharyngeal carcinoma (NPC) is frequent in Southern China, Taiwan, Borneo and polar Canada, we further tested for the possible association of the FUS2 SNP with this form of endemic cancer.]. 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:15036368
;
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:NP511982.RAV8BbcHhwd2MI_Pe9f-HCjQPAkwhZTHXzJpWVzl0Mthw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:05+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" .
}