@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP427676.RAGk5QHch96B-aMFw0FnsEdamBUb6VjAkDazEmUQzjP2c
> .
@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:NP427676.RAGk5QHch96B-aMFw0FnsEdamBUb6VjAkDazEmUQzjP2c130_head
{
this:
np:hasAssertion
dgn-np:NP427676.RAGk5QHch96B-aMFw0FnsEdamBUb6VjAkDazEmUQzjP2c130_assertion
;
np:hasProvenance
dgn-np:NP427676.RAGk5QHch96B-aMFw0FnsEdamBUb6VjAkDazEmUQzjP2c130_provenance
;
np:hasPublicationInfo
dgn-np:NP427676.RAGk5QHch96B-aMFw0FnsEdamBUb6VjAkDazEmUQzjP2c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP427676.RAGk5QHch96B-aMFw0FnsEdamBUb6VjAkDazEmUQzjP2c130_assertion
a
np:Assertion
.
dgn-np:NP427676.RAGk5QHch96B-aMFw0FnsEdamBUb6VjAkDazEmUQzjP2c130_provenance
a
np:Provenance
.
dgn-np:NP427676.RAGk5QHch96B-aMFw0FnsEdamBUb6VjAkDazEmUQzjP2c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP427676.RAGk5QHch96B-aMFw0FnsEdamBUb6VjAkDazEmUQzjP2c130_assertion
{
miriam-gene:4774
a
ncit:C16612
.
lld:C0175754
a
ncit:C7057
.
dgn-gda:DGN230f5fa110ed3553acbd4f9a0dd2b814
sio:SIO_000628
miriam-gene:4774
,
lld:C0175754
;
a
sio:SIO_001121
.
}
dgn-np:NP427676.RAGk5QHch96B-aMFw0FnsEdamBUb6VjAkDazEmUQzjP2c130_provenance
{
dgn-np:NP427676.RAGk5QHch96B-aMFw0FnsEdamBUb6VjAkDazEmUQzjP2c130_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:NP427676.RAGk5QHch96B-aMFw0FnsEdamBUb6VjAkDazEmUQzjP2c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:13+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" .
}