@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP197004.RAiOE4dORE1lTzoi88ly13biAZpugIQAftERcYZcOvnFw
> .
@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:NP197004.RAiOE4dORE1lTzoi88ly13biAZpugIQAftERcYZcOvnFw130_head
{
this:
np:hasAssertion
dgn-np:NP197004.RAiOE4dORE1lTzoi88ly13biAZpugIQAftERcYZcOvnFw130_assertion
;
np:hasProvenance
dgn-np:NP197004.RAiOE4dORE1lTzoi88ly13biAZpugIQAftERcYZcOvnFw130_provenance
;
np:hasPublicationInfo
dgn-np:NP197004.RAiOE4dORE1lTzoi88ly13biAZpugIQAftERcYZcOvnFw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP197004.RAiOE4dORE1lTzoi88ly13biAZpugIQAftERcYZcOvnFw130_assertion
a
np:Assertion
.
dgn-np:NP197004.RAiOE4dORE1lTzoi88ly13biAZpugIQAftERcYZcOvnFw130_provenance
a
np:Provenance
.
dgn-np:NP197004.RAiOE4dORE1lTzoi88ly13biAZpugIQAftERcYZcOvnFw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP197004.RAiOE4dORE1lTzoi88ly13biAZpugIQAftERcYZcOvnFw130_assertion
{
miriam-gene:182
a
ncit:C16612
.
lld:C0010278
a
ncit:C7057
.
dgn-gda:DGN1b4beecb89a23e185cca3d948f698007
sio:SIO_000628
miriam-gene:182
,
lld:C0010278
;
a
sio:SIO_001121
.
}
dgn-np:NP197004.RAiOE4dORE1lTzoi88ly13biAZpugIQAftERcYZcOvnFw130_provenance
{
dgn-np:NP197004.RAiOE4dORE1lTzoi88ly13biAZpugIQAftERcYZcOvnFw130_assertion
dcterms:description
"[That it may function in calvarial suture development and figure in the pathophysiology of craniosynostosis was suggested by the demonstration that heterozygous loss of function of JAGGED1 in humans can cause Alagille syndrome, which has craniosynostosis as a feature.]. 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:20727876
;
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:NP197004.RAiOE4dORE1lTzoi88ly13biAZpugIQAftERcYZcOvnFw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:48+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" .
}