@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A
> .
@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/v4.0.0/void/
> .
dgn-np:NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A130_head
{
this:
np:hasAssertion
dgn-np:NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A130_assertion
;
np:hasProvenance
dgn-np:NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A130_provenance
;
np:hasPublicationInfo
dgn-np:NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A130_assertion
a
np:Assertion
.
dgn-np:NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A130_provenance
a
np:Provenance
.
dgn-np:NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A130_assertion
{
miriam-gene:2132
a
ncit:C16612
.
lld:C0029423
a
ncit:C7057
.
dgn-gda:DGN39e2b47adff2d922acd0bf49feef49ef
sio:SIO_000628
miriam-gene:2132
,
lld:C0029423
;
a
sio:SIO_001121
.
}
dgn-np:NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A130_provenance
{
dgn-np:NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A130_assertion
dcterms:description
"[Although both benign conditions have been linked to defects in EXT1 or EXT2 genes, contradictory reports are present in the literature regarding the requirement of their biallelic inactivation for osteochondroma development.]. 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:20418910
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP808186.RAVVEGN7jXgEohjSQjkiX_v6OmwnXRkcEsEq1tEsf0c9A130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:51+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}