@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP742645.RAM9zjUDQHvxZJ-SiHVGsz_7OipWqKTcL8hfFTY7ebqH4
> .
@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:NP742645.RAM9zjUDQHvxZJ-SiHVGsz_7OipWqKTcL8hfFTY7ebqH4130_head
{
this:
np:hasAssertion
dgn-np:NP742645.RAM9zjUDQHvxZJ-SiHVGsz_7OipWqKTcL8hfFTY7ebqH4130_assertion
;
np:hasProvenance
dgn-np:NP742645.RAM9zjUDQHvxZJ-SiHVGsz_7OipWqKTcL8hfFTY7ebqH4130_provenance
;
np:hasPublicationInfo
dgn-np:NP742645.RAM9zjUDQHvxZJ-SiHVGsz_7OipWqKTcL8hfFTY7ebqH4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP742645.RAM9zjUDQHvxZJ-SiHVGsz_7OipWqKTcL8hfFTY7ebqH4130_assertion
a
np:Assertion
.
dgn-np:NP742645.RAM9zjUDQHvxZJ-SiHVGsz_7OipWqKTcL8hfFTY7ebqH4130_provenance
a
np:Provenance
.
dgn-np:NP742645.RAM9zjUDQHvxZJ-SiHVGsz_7OipWqKTcL8hfFTY7ebqH4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP742645.RAM9zjUDQHvxZJ-SiHVGsz_7OipWqKTcL8hfFTY7ebqH4130_assertion
{
miriam-gene:51816
a
ncit:C16612
.
lld:C0265493
a
ncit:C7057
.
dgn-gda:DGN712b182a988d4dd59d22a445dfe6318b
sio:SIO_000628
miriam-gene:51816
,
lld:C0265493
;
a
sio:SIO_001121
.
}
dgn-np:NP742645.RAM9zjUDQHvxZJ-SiHVGsz_7OipWqKTcL8hfFTY7ebqH4130_provenance
{
dgn-np:NP742645.RAM9zjUDQHvxZJ-SiHVGsz_7OipWqKTcL8hfFTY7ebqH4130_assertion
dcterms:description
"[The location of this gene in the CES critical region and its embryonic expression suggest that the overexpression of CECR1 may be responsible for at least some features of CES, particularly the heart defects.]. 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:10756095
;
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:NP742645.RAM9zjUDQHvxZJ-SiHVGsz_7OipWqKTcL8hfFTY7ebqH4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:30+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" .
}