@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP168595.RAveRIt1EzCBrjPK0eng_tqV5NPWtb35IpIQz9mImGJeo
> .
@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:NP168595.RAveRIt1EzCBrjPK0eng_tqV5NPWtb35IpIQz9mImGJeo130_head
{
this:
np:hasAssertion
dgn-np:NP168595.RAveRIt1EzCBrjPK0eng_tqV5NPWtb35IpIQz9mImGJeo130_assertion
;
np:hasProvenance
dgn-np:NP168595.RAveRIt1EzCBrjPK0eng_tqV5NPWtb35IpIQz9mImGJeo130_provenance
;
np:hasPublicationInfo
dgn-np:NP168595.RAveRIt1EzCBrjPK0eng_tqV5NPWtb35IpIQz9mImGJeo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP168595.RAveRIt1EzCBrjPK0eng_tqV5NPWtb35IpIQz9mImGJeo130_assertion
a
np:Assertion
.
dgn-np:NP168595.RAveRIt1EzCBrjPK0eng_tqV5NPWtb35IpIQz9mImGJeo130_provenance
a
np:Provenance
.
dgn-np:NP168595.RAveRIt1EzCBrjPK0eng_tqV5NPWtb35IpIQz9mImGJeo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP168595.RAveRIt1EzCBrjPK0eng_tqV5NPWtb35IpIQz9mImGJeo130_assertion
{
miriam-gene:1714
a
ncit:C16612
.
lld:C0220704
a
ncit:C7057
.
dgn-gda:DGN6566922d07452dcb0329dc0a89a62c5d
sio:SIO_000628
miriam-gene:1714
,
lld:C0220704
;
a
sio:SIO_001121
.
}
dgn-np:NP168595.RAveRIt1EzCBrjPK0eng_tqV5NPWtb35IpIQz9mImGJeo130_provenance
{
dgn-np:NP168595.RAveRIt1EzCBrjPK0eng_tqV5NPWtb35IpIQz9mImGJeo130_assertion
dcterms:description
"[Here we demonstrate that mice deficient for one type of endothelin receptor, ETA, mimic the human conditions collectively termed CATCH 22 or velocardiofacial syndrome, which include severe craniofacial deformities and defects in the cardiovascular outflow tract.]. 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:9449664
;
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:NP168595.RAveRIt1EzCBrjPK0eng_tqV5NPWtb35IpIQz9mImGJeo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:31+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" .
}