@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP911835.RARlSfL6XXDs8SHzKyymK7_MpfXKmutCX4HpaNbpsqD68
> .
@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:NP911835.RARlSfL6XXDs8SHzKyymK7_MpfXKmutCX4HpaNbpsqD68130_head
{
this:
np:hasAssertion
dgn-np:NP911835.RARlSfL6XXDs8SHzKyymK7_MpfXKmutCX4HpaNbpsqD68130_assertion
;
np:hasProvenance
dgn-np:NP911835.RARlSfL6XXDs8SHzKyymK7_MpfXKmutCX4HpaNbpsqD68130_provenance
;
np:hasPublicationInfo
dgn-np:NP911835.RARlSfL6XXDs8SHzKyymK7_MpfXKmutCX4HpaNbpsqD68130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP911835.RARlSfL6XXDs8SHzKyymK7_MpfXKmutCX4HpaNbpsqD68130_assertion
a
np:Assertion
.
dgn-np:NP911835.RARlSfL6XXDs8SHzKyymK7_MpfXKmutCX4HpaNbpsqD68130_provenance
a
np:Provenance
.
dgn-np:NP911835.RARlSfL6XXDs8SHzKyymK7_MpfXKmutCX4HpaNbpsqD68130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP911835.RARlSfL6XXDs8SHzKyymK7_MpfXKmutCX4HpaNbpsqD68130_assertion
{
miriam-gene:3198
a
ncit:C16612
.
lld:C0039685
a
ncit:C7057
.
dgn-gda:DGNcfb658038ad90936884fede1e7c629a7
sio:SIO_000628
miriam-gene:3198
,
lld:C0039685
;
a
sio:SIO_001121
.
}
dgn-np:NP911835.RARlSfL6XXDs8SHzKyymK7_MpfXKmutCX4HpaNbpsqD68130_provenance
{
dgn-np:NP911835.RARlSfL6XXDs8SHzKyymK7_MpfXKmutCX4HpaNbpsqD68130_assertion
dcterms:description
"[Hoxa1 null mice show defects such as interrupted aortic arch, aberrant subclavian artery and Tetralogy of Fallot, demonstrating that Hoxa1 is required for patterning of the great arteries and outflow tract of the heart.]. 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:21940751
;
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:NP911835.RARlSfL6XXDs8SHzKyymK7_MpfXKmutCX4HpaNbpsqD68130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:19+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" .
}