@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE
> .
@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:NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE130_head
{
this:
np:hasAssertion
dgn-np:NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE130_assertion
;
np:hasProvenance
dgn-np:NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE130_provenance
;
np:hasPublicationInfo
dgn-np:NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE130_assertion
a
np:Assertion
.
dgn-np:NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE130_provenance
a
np:Provenance
.
dgn-np:NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE130_assertion
{
miriam-gene:1403
a
ncit:C16612
.
lld:C0265303
a
ncit:C7057
.
dgn-gda:DGN9875d92f59fe01a42efa0f3352948a1c
sio:SIO_000628
miriam-gene:1403
,
lld:C0265303
;
a
sio:SIO_001121
.
}
dgn-np:NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE130_provenance
{
dgn-np:NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE130_assertion
dcterms:description
"[We present a case of Pfeiffer syndrome prenatally diagnosed at 20 weeks' gestation, in which the sonographic features of craniosynostosis, hypertelorism associated with an extreme proptosis, and broad thumb led to the diagnosis, confirmed after termination of pregnancy by dysmorphological, pathological and radiological evaluation.]. 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:15565658
;
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:NP345230.RApt_pSChGkEpmWRHVl6eafqlbAWa-o_CXjEtpZDMBaUE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:23+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" .
}