@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo
> .
@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:NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo130_head
{
this:
np:hasAssertion
dgn-np:NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo130_assertion
;
np:hasProvenance
dgn-np:NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo130_provenance
;
np:hasPublicationInfo
dgn-np:NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo130_assertion
a
np:Assertion
.
dgn-np:NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo130_provenance
a
np:Provenance
.
dgn-np:NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C1168401
a
ncit:C7057
.
dgn-gda:DGN34de116112b21821069bf73a92c6158e
sio:SIO_000628
miriam-gene:2952
,
lld:C1168401
;
a
sio:SIO_001122
.
}
dgn-np:NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo130_provenance
{
dgn-np:NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo130_assertion
dcterms:description
"[the findings suggested that the genetic polymorphisms studied are predictors of risk and are also associated with tumor recurrence, since they are important for determining the parameters associated with tumor progression and poor outcomes in HNSCC.]. 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:19442564
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP73946.RAWnHqXXTdbF_It_g6UvJVVSts31UGJLjnSBXGd2lC9mo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:36+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" .
}