@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP758590.RAbKZfjVwJTiD1Xi3O2PlUnGqIOMNL3PkdyQ6d05XY7y0
> .
@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/v3.0.0/void/
> .
dgn-np:NP758590.RAbKZfjVwJTiD1Xi3O2PlUnGqIOMNL3PkdyQ6d05XY7y0130_head
{
this:
np:hasAssertion
dgn-np:NP758590.RAbKZfjVwJTiD1Xi3O2PlUnGqIOMNL3PkdyQ6d05XY7y0130_assertion
;
np:hasProvenance
dgn-np:NP758590.RAbKZfjVwJTiD1Xi3O2PlUnGqIOMNL3PkdyQ6d05XY7y0130_provenance
;
np:hasPublicationInfo
dgn-np:NP758590.RAbKZfjVwJTiD1Xi3O2PlUnGqIOMNL3PkdyQ6d05XY7y0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP758590.RAbKZfjVwJTiD1Xi3O2PlUnGqIOMNL3PkdyQ6d05XY7y0130_assertion
a
np:Assertion
.
dgn-np:NP758590.RAbKZfjVwJTiD1Xi3O2PlUnGqIOMNL3PkdyQ6d05XY7y0130_provenance
a
np:Provenance
.
dgn-np:NP758590.RAbKZfjVwJTiD1Xi3O2PlUnGqIOMNL3PkdyQ6d05XY7y0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP758590.RAbKZfjVwJTiD1Xi3O2PlUnGqIOMNL3PkdyQ6d05XY7y0130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0004779
a
ncit:C7057
.
dgn-gda:DGNd58b674d636c12db7daa6298cafc0aea
sio:SIO_000628
miriam-gene:7248
,
lld:C0004779
;
a
sio:SIO_001121
.
}
dgn-np:NP758590.RAbKZfjVwJTiD1Xi3O2PlUnGqIOMNL3PkdyQ6d05XY7y0130_provenance
{
dgn-np:NP758590.RAbKZfjVwJTiD1Xi3O2PlUnGqIOMNL3PkdyQ6d05XY7y0130_assertion
dcterms:description
"[The gene for nevoid basal cell carcinoma syndrome (NBCCS), an autosomal dominant disorder characterized by multiple BCCs, maps to the same region and is presumed to be the tumour suppressor inactivated at this site.]. 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:8782823
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP758590.RAbKZfjVwJTiD1Xi3O2PlUnGqIOMNL3PkdyQ6d05XY7y0130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:18+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}