@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo
> .
@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:NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo130_head
{
this:
np:hasAssertion
dgn-np:NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo130_assertion
;
np:hasProvenance
dgn-np:NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo130_provenance
;
np:hasPublicationInfo
dgn-np:NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo130_assertion
a
np:Assertion
.
dgn-np:NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo130_provenance
a
np:Provenance
.
dgn-np:NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo130_assertion
{
miriam-gene:595
a
ncit:C16612
.
lld:C0007137
a
ncit:C7057
.
dgn-gda:DGN190f2a12e1bd5161e6ffae1d837e2c47
sio:SIO_000628
miriam-gene:595
,
lld:C0007137
;
a
sio:SIO_001122
.
}
dgn-np:NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo130_provenance
{
dgn-np:NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo130_assertion
dcterms:description
"[Because CCND1 plays a critical role in cell cycle control and reduced DNA repair capacity is associated with an increased risk for squamous cell carcinoma of the head and neck (SCCHN), we hypothesize that this CCND1 polymorphism modulates individual susceptibility to SCCHN.]. 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:11470749
;
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:NP47335.RA9qDwVPzek__xhS7hOlPPb5l2giRMY8VvH23n4P8rTUo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}