@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP536908.RAaKTho7buBFY8_MIzalXcREoEHBQbXLdSLKL7o31Jmnc
> .
@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:NP536908.RAaKTho7buBFY8_MIzalXcREoEHBQbXLdSLKL7o31Jmnc130_head
{
this:
np:hasAssertion
dgn-np:NP536908.RAaKTho7buBFY8_MIzalXcREoEHBQbXLdSLKL7o31Jmnc130_assertion
;
np:hasProvenance
dgn-np:NP536908.RAaKTho7buBFY8_MIzalXcREoEHBQbXLdSLKL7o31Jmnc130_provenance
;
np:hasPublicationInfo
dgn-np:NP536908.RAaKTho7buBFY8_MIzalXcREoEHBQbXLdSLKL7o31Jmnc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP536908.RAaKTho7buBFY8_MIzalXcREoEHBQbXLdSLKL7o31Jmnc130_assertion
a
np:Assertion
.
dgn-np:NP536908.RAaKTho7buBFY8_MIzalXcREoEHBQbXLdSLKL7o31Jmnc130_provenance
a
np:Provenance
.
dgn-np:NP536908.RAaKTho7buBFY8_MIzalXcREoEHBQbXLdSLKL7o31Jmnc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP536908.RAaKTho7buBFY8_MIzalXcREoEHBQbXLdSLKL7o31Jmnc130_assertion
{
miriam-gene:355
a
ncit:C16612
.
lld:C1168401
a
ncit:C7057
.
dgn-gda:DGN99e21d54faeeeba12728a0965e0c5409
sio:SIO_000628
miriam-gene:355
,
lld:C1168401
;
a
sio:SIO_001121
.
}
dgn-np:NP536908.RAaKTho7buBFY8_MIzalXcREoEHBQbXLdSLKL7o31Jmnc130_provenance
{
dgn-np:NP536908.RAaKTho7buBFY8_MIzalXcREoEHBQbXLdSLKL7o31Jmnc130_assertion
dcterms:description
"[Alteration of the FAS/FAS ligand (FASLG) pathway regulating cell death may lead to cancer development, but the effects of functional promoter polymorphisms of the FAS and FASLG genes on risk of squamous cell carcinoma of the head and neck (SCCHN) are unknown.]. 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:17000697
;
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:NP536908.RAaKTho7buBFY8_MIzalXcREoEHBQbXLdSLKL7o31Jmnc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:24+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" .
}