@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP345218.RATERYu8zX2Vn8fnIh19GyOa5tWNiT6J31RHC5xvfDiJs
> .
@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:NP345218.RATERYu8zX2Vn8fnIh19GyOa5tWNiT6J31RHC5xvfDiJs130_head
{
this:
np:hasAssertion
dgn-np:NP345218.RATERYu8zX2Vn8fnIh19GyOa5tWNiT6J31RHC5xvfDiJs130_assertion
;
np:hasProvenance
dgn-np:NP345218.RATERYu8zX2Vn8fnIh19GyOa5tWNiT6J31RHC5xvfDiJs130_provenance
;
np:hasPublicationInfo
dgn-np:NP345218.RATERYu8zX2Vn8fnIh19GyOa5tWNiT6J31RHC5xvfDiJs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP345218.RATERYu8zX2Vn8fnIh19GyOa5tWNiT6J31RHC5xvfDiJs130_assertion
a
np:Assertion
.
dgn-np:NP345218.RATERYu8zX2Vn8fnIh19GyOa5tWNiT6J31RHC5xvfDiJs130_provenance
a
np:Provenance
.
dgn-np:NP345218.RATERYu8zX2Vn8fnIh19GyOa5tWNiT6J31RHC5xvfDiJs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP345218.RATERYu8zX2Vn8fnIh19GyOa5tWNiT6J31RHC5xvfDiJs130_assertion
{
miriam-gene:10940
a
ncit:C16612
.
lld:C0410528
a
ncit:C7057
.
dgn-gda:DGN59763ff424b70fdcbdbf6a9ac9cae035
sio:SIO_000628
miriam-gene:10940
,
lld:C0410528
;
a
sio:SIO_001121
.
}
dgn-np:NP345218.RATERYu8zX2Vn8fnIh19GyOa5tWNiT6J31RHC5xvfDiJs130_provenance
{
dgn-np:NP345218.RATERYu8zX2Vn8fnIh19GyOa5tWNiT6J31RHC5xvfDiJs130_assertion
dcterms:description
"[We demonstrate that these mutations impair the integrity and activity of this complex and that they impair cell proliferation, providing likely molecular and cellular mechanisms by which POP1 mutations cause this severe skeletal dysplasia.]. 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:21455487
;
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:NP345218.RATERYu8zX2Vn8fnIh19GyOa5tWNiT6J31RHC5xvfDiJs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:23+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" .
}