@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP879462.RARBpixXh9F5x0KAs3lpMMZnnD5ZiEiI6angSdmlS5VpU
> .
@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:NP879462.RARBpixXh9F5x0KAs3lpMMZnnD5ZiEiI6angSdmlS5VpU130_head
{
this:
np:hasAssertion
dgn-np:NP879462.RARBpixXh9F5x0KAs3lpMMZnnD5ZiEiI6angSdmlS5VpU130_assertion
;
np:hasProvenance
dgn-np:NP879462.RARBpixXh9F5x0KAs3lpMMZnnD5ZiEiI6angSdmlS5VpU130_provenance
;
np:hasPublicationInfo
dgn-np:NP879462.RARBpixXh9F5x0KAs3lpMMZnnD5ZiEiI6angSdmlS5VpU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP879462.RARBpixXh9F5x0KAs3lpMMZnnD5ZiEiI6angSdmlS5VpU130_assertion
a
np:Assertion
.
dgn-np:NP879462.RARBpixXh9F5x0KAs3lpMMZnnD5ZiEiI6angSdmlS5VpU130_provenance
a
np:Provenance
.
dgn-np:NP879462.RARBpixXh9F5x0KAs3lpMMZnnD5ZiEiI6angSdmlS5VpU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP879462.RARBpixXh9F5x0KAs3lpMMZnnD5ZiEiI6angSdmlS5VpU130_assertion
{
miriam-gene:4484
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGNd2c891c46c0f4e11d7ef4c2b083a0a09
sio:SIO_000628
miriam-gene:4484
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP879462.RARBpixXh9F5x0KAs3lpMMZnnD5ZiEiI6angSdmlS5VpU130_provenance
{
dgn-np:NP879462.RARBpixXh9F5x0KAs3lpMMZnnD5ZiEiI6angSdmlS5VpU130_assertion
dcterms:description
"[Familial predisposition to basal cell carcinoma (BCC) and squamous cell carcinoma (SCC) of the skin are apparent in the autosomal dominant syndromes naevoid basal cell carcinoma syndrome (NBCCS) and multiple self-healing squamous epitheliomata (MSSE) respectively.]. 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:8688329
;
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:NP879462.RARBpixXh9F5x0KAs3lpMMZnnD5ZiEiI6angSdmlS5VpU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:57+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" .
}