@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP533484.RA9Jpm7xvEgmxMbUebcbzqOSiLbBXWw3kYsefyWuPCQC8
> .
@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:NP533484.RA9Jpm7xvEgmxMbUebcbzqOSiLbBXWw3kYsefyWuPCQC8130_head
{
this:
np:hasAssertion
dgn-np:NP533484.RA9Jpm7xvEgmxMbUebcbzqOSiLbBXWw3kYsefyWuPCQC8130_assertion
;
np:hasProvenance
dgn-np:NP533484.RA9Jpm7xvEgmxMbUebcbzqOSiLbBXWw3kYsefyWuPCQC8130_provenance
;
np:hasPublicationInfo
dgn-np:NP533484.RA9Jpm7xvEgmxMbUebcbzqOSiLbBXWw3kYsefyWuPCQC8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP533484.RA9Jpm7xvEgmxMbUebcbzqOSiLbBXWw3kYsefyWuPCQC8130_assertion
a
np:Assertion
.
dgn-np:NP533484.RA9Jpm7xvEgmxMbUebcbzqOSiLbBXWw3kYsefyWuPCQC8130_provenance
a
np:Provenance
.
dgn-np:NP533484.RA9Jpm7xvEgmxMbUebcbzqOSiLbBXWw3kYsefyWuPCQC8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP533484.RA9Jpm7xvEgmxMbUebcbzqOSiLbBXWw3kYsefyWuPCQC8130_assertion
{
miriam-gene:1403
a
ncit:C16612
.
lld:C0001193
a
ncit:C7057
.
dgn-gda:DGNa6108194307cde8e930ad3c62c290b66
sio:SIO_000628
miriam-gene:1403
,
lld:C0001193
;
a
sio:SIO_001121
.
}
dgn-np:NP533484.RA9Jpm7xvEgmxMbUebcbzqOSiLbBXWw3kYsefyWuPCQC8130_provenance
{
dgn-np:NP533484.RA9Jpm7xvEgmxMbUebcbzqOSiLbBXWw3kYsefyWuPCQC8130_assertion
dcterms:description
"[Our report demonstrates the feasibility of the prenatal diagnosis of Apert syndrome with cloverleaf skull using ultrasound, fetal magnetic resonance imaging and mutation analysis, and also highlights the importance of the biparietal diameter as an early predictor of growth restriction in severe craniosynostosis cases.]. 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:19940464
;
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:NP533484.RA9Jpm7xvEgmxMbUebcbzqOSiLbBXWw3kYsefyWuPCQC8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:22+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" .
}