@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP615129.RAAty-1-YQODaYvXuFLSAuvwQdn8vmlNupRvoWUBPxk7E
> .
@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:NP615129.RAAty-1-YQODaYvXuFLSAuvwQdn8vmlNupRvoWUBPxk7E130_head
{
this:
np:hasAssertion
dgn-np:NP615129.RAAty-1-YQODaYvXuFLSAuvwQdn8vmlNupRvoWUBPxk7E130_assertion
;
np:hasProvenance
dgn-np:NP615129.RAAty-1-YQODaYvXuFLSAuvwQdn8vmlNupRvoWUBPxk7E130_provenance
;
np:hasPublicationInfo
dgn-np:NP615129.RAAty-1-YQODaYvXuFLSAuvwQdn8vmlNupRvoWUBPxk7E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP615129.RAAty-1-YQODaYvXuFLSAuvwQdn8vmlNupRvoWUBPxk7E130_assertion
a
np:Assertion
.
dgn-np:NP615129.RAAty-1-YQODaYvXuFLSAuvwQdn8vmlNupRvoWUBPxk7E130_provenance
a
np:Provenance
.
dgn-np:NP615129.RAAty-1-YQODaYvXuFLSAuvwQdn8vmlNupRvoWUBPxk7E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP615129.RAAty-1-YQODaYvXuFLSAuvwQdn8vmlNupRvoWUBPxk7E130_assertion
{
miriam-gene:2261
a
ncit:C16612
.
lld:C0022603
a
ncit:C7057
.
dgn-gda:DGN6d83340128e091f123406af148e59f66
sio:SIO_000628
miriam-gene:2261
,
lld:C0022603
;
a
sio:SIO_001121
.
}
dgn-np:NP615129.RAAty-1-YQODaYvXuFLSAuvwQdn8vmlNupRvoWUBPxk7E130_provenance
{
dgn-np:NP615129.RAAty-1-YQODaYvXuFLSAuvwQdn8vmlNupRvoWUBPxk7E130_assertion
dcterms:description
"[Because FGFR3 and PIK3CA mutations have been reported to be involved in the pathogenesis of sporadic SK, we analysed five SKs of an affected family member for hotspot mutations of these genes.]. 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:18503601
;
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:NP615129.RAAty-1-YQODaYvXuFLSAuvwQdn8vmlNupRvoWUBPxk7E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:12+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" .
}