@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP815168.RATvsJ0W38_sp-UDL-VwtwX8tIamOo4X6Td39Cbb0Z950
> .
@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:NP815168.RATvsJ0W38_sp-UDL-VwtwX8tIamOo4X6Td39Cbb0Z950130_head
{
this:
np:hasAssertion
dgn-np:NP815168.RATvsJ0W38_sp-UDL-VwtwX8tIamOo4X6Td39Cbb0Z950130_assertion
;
np:hasProvenance
dgn-np:NP815168.RATvsJ0W38_sp-UDL-VwtwX8tIamOo4X6Td39Cbb0Z950130_provenance
;
np:hasPublicationInfo
dgn-np:NP815168.RATvsJ0W38_sp-UDL-VwtwX8tIamOo4X6Td39Cbb0Z950130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP815168.RATvsJ0W38_sp-UDL-VwtwX8tIamOo4X6Td39Cbb0Z950130_assertion
a
np:Assertion
.
dgn-np:NP815168.RATvsJ0W38_sp-UDL-VwtwX8tIamOo4X6Td39Cbb0Z950130_provenance
a
np:Provenance
.
dgn-np:NP815168.RATvsJ0W38_sp-UDL-VwtwX8tIamOo4X6Td39Cbb0Z950130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP815168.RATvsJ0W38_sp-UDL-VwtwX8tIamOo4X6Td39Cbb0Z950130_assertion
{
miriam-gene:11107
a
ncit:C16612
.
lld:C0268344
a
ncit:C7057
.
dgn-gda:DGNe193a054684d342abb4e4a18c2485a6d
sio:SIO_000628
miriam-gene:11107
,
lld:C0268344
;
a
sio:SIO_001121
.
}
dgn-np:NP815168.RATvsJ0W38_sp-UDL-VwtwX8tIamOo4X6Td39Cbb0Z950130_provenance
{
dgn-np:NP815168.RATvsJ0W38_sp-UDL-VwtwX8tIamOo4X6Td39Cbb0Z950130_assertion
dcterms:description
"[Transcriptional regulation of extracellular matrix components, particularly of fibrillar collagens, by PRDM5 and ZNF469 suggests that they might be part of the same pathway, the disruption of which is likely to cause the features of BCS.]. 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:23680354
;
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:NP815168.RATvsJ0W38_sp-UDL-VwtwX8tIamOo4X6Td39Cbb0Z950130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:19+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" .
}