@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP445421.RAimDVkBLI6Tm7pmGgdCLhLnmwFp71TpU0fc2Nr1tJPIQ
> .
@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:NP445421.RAimDVkBLI6Tm7pmGgdCLhLnmwFp71TpU0fc2Nr1tJPIQ130_head
{
this:
np:hasAssertion
dgn-np:NP445421.RAimDVkBLI6Tm7pmGgdCLhLnmwFp71TpU0fc2Nr1tJPIQ130_assertion
;
np:hasProvenance
dgn-np:NP445421.RAimDVkBLI6Tm7pmGgdCLhLnmwFp71TpU0fc2Nr1tJPIQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP445421.RAimDVkBLI6Tm7pmGgdCLhLnmwFp71TpU0fc2Nr1tJPIQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP445421.RAimDVkBLI6Tm7pmGgdCLhLnmwFp71TpU0fc2Nr1tJPIQ130_assertion
a
np:Assertion
.
dgn-np:NP445421.RAimDVkBLI6Tm7pmGgdCLhLnmwFp71TpU0fc2Nr1tJPIQ130_provenance
a
np:Provenance
.
dgn-np:NP445421.RAimDVkBLI6Tm7pmGgdCLhLnmwFp71TpU0fc2Nr1tJPIQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP445421.RAimDVkBLI6Tm7pmGgdCLhLnmwFp71TpU0fc2Nr1tJPIQ130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0004779
a
ncit:C7057
.
dgn-gda:DGN39a6af94d7565b74f8293d664b57540f
sio:SIO_000628
miriam-gene:5979
,
lld:C0004779
;
a
sio:SIO_001121
.
}
dgn-np:NP445421.RAimDVkBLI6Tm7pmGgdCLhLnmwFp71TpU0fc2Nr1tJPIQ130_provenance
{
dgn-np:NP445421.RAimDVkBLI6Tm7pmGgdCLhLnmwFp71TpU0fc2Nr1tJPIQ130_assertion
dcterms:description
"[We have screened the 23 PTC exons for mutations using single strand conformation polymorphism analysis of DNA from 86 basal cell nevus syndrome probands, 26 sporadic basal cell carcinomas, and seven basal cell nevus syndrome-associated basal cell carcinomas.]. 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:9620294
;
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:NP445421.RAimDVkBLI6Tm7pmGgdCLhLnmwFp71TpU0fc2Nr1tJPIQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:25+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" .
}