@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP462848.RAQ9M8v24z5SdcRn8WX318bbsWOvn1wqcPYQuTTTWB61g
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP462848.RAQ9M8v24z5SdcRn8WX318bbsWOvn1wqcPYQuTTTWB61g130_head
{
this:
np:hasAssertion
dgn-np:NP462848.RAQ9M8v24z5SdcRn8WX318bbsWOvn1wqcPYQuTTTWB61g130_assertion
;
np:hasProvenance
dgn-np:NP462848.RAQ9M8v24z5SdcRn8WX318bbsWOvn1wqcPYQuTTTWB61g130_provenance
;
np:hasPublicationInfo
dgn-np:NP462848.RAQ9M8v24z5SdcRn8WX318bbsWOvn1wqcPYQuTTTWB61g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP462848.RAQ9M8v24z5SdcRn8WX318bbsWOvn1wqcPYQuTTTWB61g130_assertion
a
np:Assertion
.
dgn-np:NP462848.RAQ9M8v24z5SdcRn8WX318bbsWOvn1wqcPYQuTTTWB61g130_provenance
a
np:Provenance
.
dgn-np:NP462848.RAQ9M8v24z5SdcRn8WX318bbsWOvn1wqcPYQuTTTWB61g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP462848.RAQ9M8v24z5SdcRn8WX318bbsWOvn1wqcPYQuTTTWB61g130_assertion
{
miriam-gene:3211
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGNd197db4cb66525100b30aecaacc73938
sio:SIO_000628
miriam-gene:3211
,
lld:C0004352
;
a
sio:SIO_001121
.
}
dgn-np:NP462848.RAQ9M8v24z5SdcRn8WX318bbsWOvn1wqcPYQuTTTWB61g130_provenance
{
dgn-np:NP462848.RAQ9M8v24z5SdcRn8WX318bbsWOvn1wqcPYQuTTTWB61g130_assertion
dcterms:description
"[Mice with null mutations of Hoxa1 or Hoxb1, two genes critical to hindbrain development, have phenotypic features frequently observed in autism, but no naturally occurring variants of either gene have been identified in mammals.]. 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:11091361
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP462848.RAQ9M8v24z5SdcRn8WX318bbsWOvn1wqcPYQuTTTWB61g130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:12+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}