@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP90484.RAeLLULQ8Eyu7m23NB9t5sa_301HY7ztez5i0W5KM2nBE
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP90484.RAeLLULQ8Eyu7m23NB9t5sa_301HY7ztez5i0W5KM2nBE130_head
{
this:
np:hasAssertion
dgn-np:NP90484.RAeLLULQ8Eyu7m23NB9t5sa_301HY7ztez5i0W5KM2nBE130_assertion
;
np:hasProvenance
dgn-np:NP90484.RAeLLULQ8Eyu7m23NB9t5sa_301HY7ztez5i0W5KM2nBE130_provenance
;
np:hasPublicationInfo
dgn-np:NP90484.RAeLLULQ8Eyu7m23NB9t5sa_301HY7ztez5i0W5KM2nBE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP90484.RAeLLULQ8Eyu7m23NB9t5sa_301HY7ztez5i0W5KM2nBE130_assertion
a
np:Assertion
.
dgn-np:NP90484.RAeLLULQ8Eyu7m23NB9t5sa_301HY7ztez5i0W5KM2nBE130_provenance
a
np:Provenance
.
dgn-np:NP90484.RAeLLULQ8Eyu7m23NB9t5sa_301HY7ztez5i0W5KM2nBE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP90484.RAeLLULQ8Eyu7m23NB9t5sa_301HY7ztez5i0W5KM2nBE130_assertion
{
miriam-gene:595
a
ncit:C16612
.
lld:C0153381
a
ncit:C7057
.
dgn-gda:DGNe45cc8268af7c65e2790bff2f799221d
sio:SIO_000628
miriam-gene:595
,
lld:C0153381
;
a
sio:SIO_001122
.
}
dgn-np:NP90484.RAeLLULQ8Eyu7m23NB9t5sa_301HY7ztez5i0W5KM2nBE130_provenance
{
dgn-np:NP90484.RAeLLULQ8Eyu7m23NB9t5sa_301HY7ztez5i0W5KM2nBE130_assertion
dcterms:description
"[Our data suggests that the CCND1 GG(870) genotype is associated with increased susceptibility to OSCC. The involvement of cyclin D1 polymorphism in mechanisms of SCC development may differ in the different sub-sites of the head and neck.]. 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:15695117
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP90484.RAeLLULQ8Eyu7m23NB9t5sa_301HY7ztez5i0W5KM2nBE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:29+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}