@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k
> .
@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:NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_head
{
this:
np:hasAssertion
dgn-np:NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_assertion
;
np:hasProvenance
dgn-np:NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_provenance
;
np:hasPublicationInfo
dgn-np:NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_assertion
a
np:Assertion
.
dgn-np:NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_provenance
a
np:Provenance
.
dgn-np:NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_assertion
{
miriam-gene:3586
a
ncit:C16612
.
lld:C0266449
a
ncit:C7057
.
dgn-gda:DGN45b2093de4c3e2046dfe61c1050a641e
sio:SIO_000628
miriam-gene:3586
,
lld:C0266449
;
a
sio:SIO_001121
.
}
dgn-np:NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_provenance
{
dgn-np:NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_assertion
dcterms:description
"[The study focused on the associated brain malformations, including neuronal migration defects, which predominated in individuals with ZIC2 mutations, and neural tube defects, which were frequently associated with ZIC2 (rachischisis) and TGIF mutations.]. 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:21940735
;
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:NP298935.RAYoXTj1uU8LFiynO3JkhnYvS3HEnC8dfB6oXMp5_Vt8k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:50+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" .
}