@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP536516.RAqzbZ556pYwepb0UwSNnOfevY_KeKLCjhuO6LseNfsWM
> .
@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:NP536516.RAqzbZ556pYwepb0UwSNnOfevY_KeKLCjhuO6LseNfsWM130_head
{
this:
np:hasAssertion
dgn-np:NP536516.RAqzbZ556pYwepb0UwSNnOfevY_KeKLCjhuO6LseNfsWM130_assertion
;
np:hasProvenance
dgn-np:NP536516.RAqzbZ556pYwepb0UwSNnOfevY_KeKLCjhuO6LseNfsWM130_provenance
;
np:hasPublicationInfo
dgn-np:NP536516.RAqzbZ556pYwepb0UwSNnOfevY_KeKLCjhuO6LseNfsWM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP536516.RAqzbZ556pYwepb0UwSNnOfevY_KeKLCjhuO6LseNfsWM130_assertion
a
np:Assertion
.
dgn-np:NP536516.RAqzbZ556pYwepb0UwSNnOfevY_KeKLCjhuO6LseNfsWM130_provenance
a
np:Provenance
.
dgn-np:NP536516.RAqzbZ556pYwepb0UwSNnOfevY_KeKLCjhuO6LseNfsWM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP536516.RAqzbZ556pYwepb0UwSNnOfevY_KeKLCjhuO6LseNfsWM130_assertion
{
miriam-gene:89884
a
ncit:C16612
.
lld:C0599750
a
ncit:C7057
.
dgn-gda:DGNd51b2602b239f5b508a5dbd088fca49e
sio:SIO_000628
miriam-gene:89884
,
lld:C0599750
;
a
sio:SIO_001121
.
}
dgn-np:NP536516.RAqzbZ556pYwepb0UwSNnOfevY_KeKLCjhuO6LseNfsWM130_provenance
{
dgn-np:NP536516.RAqzbZ556pYwepb0UwSNnOfevY_KeKLCjhuO6LseNfsWM130_assertion
dcterms:description
"[Since the CPHD with pituitary stalk interruption cannot be due to HESX1, LHX4 or OTX2 mutation in our case, other pathogenetic mechanisms may be responsible for CPHD associated with unilateral ICA agenesis.]. 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:22797803
;
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:NP536516.RAqzbZ556pYwepb0UwSNnOfevY_KeKLCjhuO6LseNfsWM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:23+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" .
}