@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP786106.RAlZdeIYmqmiOlidLoKr9N1YrQHuH2qJthelrZON_8Z_Y
> .
@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:NP786106.RAlZdeIYmqmiOlidLoKr9N1YrQHuH2qJthelrZON_8Z_Y130_head
{
this:
np:hasAssertion
dgn-np:NP786106.RAlZdeIYmqmiOlidLoKr9N1YrQHuH2qJthelrZON_8Z_Y130_assertion
;
np:hasProvenance
dgn-np:NP786106.RAlZdeIYmqmiOlidLoKr9N1YrQHuH2qJthelrZON_8Z_Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP786106.RAlZdeIYmqmiOlidLoKr9N1YrQHuH2qJthelrZON_8Z_Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP786106.RAlZdeIYmqmiOlidLoKr9N1YrQHuH2qJthelrZON_8Z_Y130_assertion
a
np:Assertion
.
dgn-np:NP786106.RAlZdeIYmqmiOlidLoKr9N1YrQHuH2qJthelrZON_8Z_Y130_provenance
a
np:Provenance
.
dgn-np:NP786106.RAlZdeIYmqmiOlidLoKr9N1YrQHuH2qJthelrZON_8Z_Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP786106.RAlZdeIYmqmiOlidLoKr9N1YrQHuH2qJthelrZON_8Z_Y130_assertion
{
miriam-gene:57493
a
ncit:C16612
.
lld:C2919945
a
ncit:C7057
.
dgn-gda:DGNe35e13a2463bd2fa4ea2d69d08f5e7e9
sio:SIO_000628
miriam-gene:57493
,
lld:C2919945
;
a
sio:SIO_001121
.
}
dgn-np:NP786106.RAlZdeIYmqmiOlidLoKr9N1YrQHuH2qJthelrZON_8Z_Y130_provenance
{
dgn-np:NP786106.RAlZdeIYmqmiOlidLoKr9N1YrQHuH2qJthelrZON_8Z_Y130_assertion
dcterms:description
"[Defects in the hearts of zebrafish lacking heg or ccm2, in the aortas of early mouse embryos lacking CCM2 and in the lymphatic vessels of neonatal mice lacking HEG1 were associated with abnormal endothelial cell junctions like those observed in human CCMs.]. 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:19151727
;
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:NP786106.RAlZdeIYmqmiOlidLoKr9N1YrQHuH2qJthelrZON_8Z_Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:56+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" .
}