@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP322831.RAMSgdOHYUiz_b1fEnEVG_bx04OcP682H3dyRENtI3sYs
> .
@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:NP322831.RAMSgdOHYUiz_b1fEnEVG_bx04OcP682H3dyRENtI3sYs130_head
{
this:
np:hasAssertion
dgn-np:NP322831.RAMSgdOHYUiz_b1fEnEVG_bx04OcP682H3dyRENtI3sYs130_assertion
;
np:hasProvenance
dgn-np:NP322831.RAMSgdOHYUiz_b1fEnEVG_bx04OcP682H3dyRENtI3sYs130_provenance
;
np:hasPublicationInfo
dgn-np:NP322831.RAMSgdOHYUiz_b1fEnEVG_bx04OcP682H3dyRENtI3sYs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP322831.RAMSgdOHYUiz_b1fEnEVG_bx04OcP682H3dyRENtI3sYs130_assertion
a
np:Assertion
.
dgn-np:NP322831.RAMSgdOHYUiz_b1fEnEVG_bx04OcP682H3dyRENtI3sYs130_provenance
a
np:Provenance
.
dgn-np:NP322831.RAMSgdOHYUiz_b1fEnEVG_bx04OcP682H3dyRENtI3sYs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP322831.RAMSgdOHYUiz_b1fEnEVG_bx04OcP682H3dyRENtI3sYs130_assertion
{
miriam-gene:2131
a
ncit:C16612
.
lld:C0029423
a
ncit:C7057
.
dgn-gda:DGNce23422bec1ae57f1f63e789bc3bd990
sio:SIO_000628
miriam-gene:2131
,
lld:C0029423
;
a
sio:SIO_001121
.
}
dgn-np:NP322831.RAMSgdOHYUiz_b1fEnEVG_bx04OcP682H3dyRENtI3sYs130_provenance
{
dgn-np:NP322831.RAMSgdOHYUiz_b1fEnEVG_bx04OcP682H3dyRENtI3sYs130_assertion
dcterms:description
"[Reduced EXT1 or EXT2 expression in osteochondromas is associated with disordered cellular distribution of HSPGs, resulting in defective endochondral ossification which is likely to be involved in the formation of osteochondromas.]. 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:18853760
;
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:NP322831.RAMSgdOHYUiz_b1fEnEVG_bx04OcP682H3dyRENtI3sYs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:09+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" .
}