@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP560400.RAOBzdy2NiUvoAK-sReUdGDgiqE5yAnqKGbkDmtwXZfis
> .
@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:NP560400.RAOBzdy2NiUvoAK-sReUdGDgiqE5yAnqKGbkDmtwXZfis130_head
{
this:
np:hasAssertion
dgn-np:NP560400.RAOBzdy2NiUvoAK-sReUdGDgiqE5yAnqKGbkDmtwXZfis130_assertion
;
np:hasProvenance
dgn-np:NP560400.RAOBzdy2NiUvoAK-sReUdGDgiqE5yAnqKGbkDmtwXZfis130_provenance
;
np:hasPublicationInfo
dgn-np:NP560400.RAOBzdy2NiUvoAK-sReUdGDgiqE5yAnqKGbkDmtwXZfis130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP560400.RAOBzdy2NiUvoAK-sReUdGDgiqE5yAnqKGbkDmtwXZfis130_assertion
a
np:Assertion
.
dgn-np:NP560400.RAOBzdy2NiUvoAK-sReUdGDgiqE5yAnqKGbkDmtwXZfis130_provenance
a
np:Provenance
.
dgn-np:NP560400.RAOBzdy2NiUvoAK-sReUdGDgiqE5yAnqKGbkDmtwXZfis130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP560400.RAOBzdy2NiUvoAK-sReUdGDgiqE5yAnqKGbkDmtwXZfis130_assertion
{
miriam-gene:1637
a
ncit:C16612
.
lld:C0041107
a
ncit:C7057
.
dgn-gda:DGNb2f91185ef8e88c569783d6c85d7cdd9
sio:SIO_000628
miriam-gene:1637
,
lld:C0041107
;
a
sio:SIO_001121
.
}
dgn-np:NP560400.RAOBzdy2NiUvoAK-sReUdGDgiqE5yAnqKGbkDmtwXZfis130_provenance
{
dgn-np:NP560400.RAOBzdy2NiUvoAK-sReUdGDgiqE5yAnqKGbkDmtwXZfis130_assertion
dcterms:description
"[We used chromosome engineering to create mice that were trisomic or monosomic for only the mouse chromosome segment orthologous to the DSCR and assessed dysmorphologies of the craniofacial skeleton that show direct parallels with DS in mice with a larger segmental trisomy.]. 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:15499018
;
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:NP560400.RAOBzdy2NiUvoAK-sReUdGDgiqE5yAnqKGbkDmtwXZfis130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:38+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" .
}