@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP401358.RAWSsHKjizSMXzz1AZj0MiTcsh7d_TJde62ZVLTAgT4jQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP401358.RAWSsHKjizSMXzz1AZj0MiTcsh7d_TJde62ZVLTAgT4jQ130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP401358.RAWSsHKjizSMXzz1AZj0MiTcsh7d_TJde62ZVLTAgT4jQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP401358.RAWSsHKjizSMXzz1AZj0MiTcsh7d_TJde62ZVLTAgT4jQ130_assertion
a
np:Assertion
.
dgn-np:NP401358.RAWSsHKjizSMXzz1AZj0MiTcsh7d_TJde62ZVLTAgT4jQ130_provenance
a
np:Provenance
.
dgn-np:NP401358.RAWSsHKjizSMXzz1AZj0MiTcsh7d_TJde62ZVLTAgT4jQ130_publicationInfo
a
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.
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dgn-np:NP401358.RAWSsHKjizSMXzz1AZj0MiTcsh7d_TJde62ZVLTAgT4jQ130_assertion
{
miriam-gene:2263
a
ncit:C16612
.
lld:C0001193
a
ncit:C7057
.
dgn-gda:DGNe9813a7b9d9d94089a89c9e5a721c090
sio:SIO_000628
miriam-gene:2263
,
lld:C0001193
;
a
sio:SIO_001122
.
}
dgn-np:NP401358.RAWSsHKjizSMXzz1AZj0MiTcsh7d_TJde62ZVLTAgT4jQ130_provenance
{
dgn-np:NP401358.RAWSsHKjizSMXzz1AZj0MiTcsh7d_TJde62ZVLTAgT4jQ130_assertion
dcterms:description
"[We examine late embryonic skull development and suture patency in Fgfr2 Apert syndrome mice between embryonic day 17.5 and birth and quantify the effects of these mutations on 3D skull morphology, suture patency and growth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:24580805
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP401358.RAWSsHKjizSMXzz1AZj0MiTcsh7d_TJde62ZVLTAgT4jQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:33+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
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;
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
"v3.0.0.0" .
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pav:version
"v3.0.0" .
}