@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP854248.RAUy6ihmFYWHarWJHalxVROaQoOyP4RdMwTARDnnIDRXs
> .
@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:NP854248.RAUy6ihmFYWHarWJHalxVROaQoOyP4RdMwTARDnnIDRXs130_head
{
this:
np:hasAssertion
dgn-np:NP854248.RAUy6ihmFYWHarWJHalxVROaQoOyP4RdMwTARDnnIDRXs130_assertion
;
np:hasProvenance
dgn-np:NP854248.RAUy6ihmFYWHarWJHalxVROaQoOyP4RdMwTARDnnIDRXs130_provenance
;
np:hasPublicationInfo
dgn-np:NP854248.RAUy6ihmFYWHarWJHalxVROaQoOyP4RdMwTARDnnIDRXs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP854248.RAUy6ihmFYWHarWJHalxVROaQoOyP4RdMwTARDnnIDRXs130_assertion
a
np:Assertion
.
dgn-np:NP854248.RAUy6ihmFYWHarWJHalxVROaQoOyP4RdMwTARDnnIDRXs130_provenance
a
np:Provenance
.
dgn-np:NP854248.RAUy6ihmFYWHarWJHalxVROaQoOyP4RdMwTARDnnIDRXs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP854248.RAUy6ihmFYWHarWJHalxVROaQoOyP4RdMwTARDnnIDRXs130_assertion
{
miriam-gene:5015
a
ncit:C16612
.
lld:C0935572
a
ncit:C7057
.
dgn-gda:DGNef06db9427d0c90537f7590e70d63f7a
sio:SIO_000628
miriam-gene:5015
,
lld:C0935572
;
a
sio:SIO_001121
.
}
dgn-np:NP854248.RAUy6ihmFYWHarWJHalxVROaQoOyP4RdMwTARDnnIDRXs130_provenance
{
dgn-np:NP854248.RAUy6ihmFYWHarWJHalxVROaQoOyP4RdMwTARDnnIDRXs130_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:NP854248.RAUy6ihmFYWHarWJHalxVROaQoOyP4RdMwTARDnnIDRXs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:42+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" .
}