@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP658296.RAFXd-8uQxH2YXkO0WnGCSOB0M_fsZgUWo5IuTQRjhgDg
> .
@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:NP658296.RAFXd-8uQxH2YXkO0WnGCSOB0M_fsZgUWo5IuTQRjhgDg130_head
{
this:
np:hasAssertion
dgn-np:NP658296.RAFXd-8uQxH2YXkO0WnGCSOB0M_fsZgUWo5IuTQRjhgDg130_assertion
;
np:hasProvenance
dgn-np:NP658296.RAFXd-8uQxH2YXkO0WnGCSOB0M_fsZgUWo5IuTQRjhgDg130_provenance
;
np:hasPublicationInfo
dgn-np:NP658296.RAFXd-8uQxH2YXkO0WnGCSOB0M_fsZgUWo5IuTQRjhgDg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP658296.RAFXd-8uQxH2YXkO0WnGCSOB0M_fsZgUWo5IuTQRjhgDg130_assertion
a
np:Assertion
.
dgn-np:NP658296.RAFXd-8uQxH2YXkO0WnGCSOB0M_fsZgUWo5IuTQRjhgDg130_provenance
a
np:Provenance
.
dgn-np:NP658296.RAFXd-8uQxH2YXkO0WnGCSOB0M_fsZgUWo5IuTQRjhgDg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP658296.RAFXd-8uQxH2YXkO0WnGCSOB0M_fsZgUWo5IuTQRjhgDg130_assertion
{
miriam-gene:4781
a
ncit:C16612
.
lld:C0020255
a
ncit:C7057
.
dgn-gda:DGN4cb27aac40aff09b2107e6327d49bdf8
sio:SIO_000628
miriam-gene:4781
,
lld:C0020255
;
a
sio:SIO_001121
.
}
dgn-np:NP658296.RAFXd-8uQxH2YXkO0WnGCSOB0M_fsZgUWo5IuTQRjhgDg130_provenance
{
dgn-np:NP658296.RAFXd-8uQxH2YXkO0WnGCSOB0M_fsZgUWo5IuTQRjhgDg130_assertion
dcterms:description
"[It was shown that loss of NFIA results in hydrocephalus and agenesis of the corpus callosum and that NFIB deficiency leads to neurological defects and to severe lung hypoplasia, whereas Nfic knockout mice exhibit specific tooth 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:17353270
;
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:NP658296.RAFXd-8uQxH2YXkO0WnGCSOB0M_fsZgUWo5IuTQRjhgDg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:36+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" .
}