@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP874004.RAYifqgVzOl_0i4ZHQLLxpZ0wGSDQuztdld97Pj8PP1dU
> .
@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:NP874004.RAYifqgVzOl_0i4ZHQLLxpZ0wGSDQuztdld97Pj8PP1dU130_head
{
this:
np:hasAssertion
dgn-np:NP874004.RAYifqgVzOl_0i4ZHQLLxpZ0wGSDQuztdld97Pj8PP1dU130_assertion
;
np:hasProvenance
dgn-np:NP874004.RAYifqgVzOl_0i4ZHQLLxpZ0wGSDQuztdld97Pj8PP1dU130_provenance
;
np:hasPublicationInfo
dgn-np:NP874004.RAYifqgVzOl_0i4ZHQLLxpZ0wGSDQuztdld97Pj8PP1dU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP874004.RAYifqgVzOl_0i4ZHQLLxpZ0wGSDQuztdld97Pj8PP1dU130_assertion
a
np:Assertion
.
dgn-np:NP874004.RAYifqgVzOl_0i4ZHQLLxpZ0wGSDQuztdld97Pj8PP1dU130_provenance
a
np:Provenance
.
dgn-np:NP874004.RAYifqgVzOl_0i4ZHQLLxpZ0wGSDQuztdld97Pj8PP1dU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP874004.RAYifqgVzOl_0i4ZHQLLxpZ0wGSDQuztdld97Pj8PP1dU130_assertion
{
miriam-gene:2261
a
ncit:C16612
.
lld:C0007137
a
ncit:C7057
.
dgn-gda:DGN35bf35f042de817d72f15e23b163d3ae
sio:SIO_000628
miriam-gene:2261
,
lld:C0007137
;
a
sio:SIO_001121
.
}
dgn-np:NP874004.RAYifqgVzOl_0i4ZHQLLxpZ0wGSDQuztdld97Pj8PP1dU130_provenance
{
dgn-np:NP874004.RAYifqgVzOl_0i4ZHQLLxpZ0wGSDQuztdld97Pj8PP1dU130_assertion
dcterms:description
"[We investigated the activation of FGFR3 and OIS by mutation and immunohistochemical analysis in skin tumours, including seborrhoeic keratosis, actinic keratosis (AK), Bowen's disease (BD), basal cell carcinoma (BCC) and squamous cell carcinoma (SCC).]. 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:19298285
;
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:NP874004.RAYifqgVzOl_0i4ZHQLLxpZ0wGSDQuztdld97Pj8PP1dU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:54+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" .
}