@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP635109.RA2ycOaGvOmhGFsGxdT-htG6-iOxMRuw20TwEd-Hy-aqc
> .
@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:NP635109.RA2ycOaGvOmhGFsGxdT-htG6-iOxMRuw20TwEd-Hy-aqc130_head
{
this:
np:hasAssertion
dgn-np:NP635109.RA2ycOaGvOmhGFsGxdT-htG6-iOxMRuw20TwEd-Hy-aqc130_assertion
;
np:hasProvenance
dgn-np:NP635109.RA2ycOaGvOmhGFsGxdT-htG6-iOxMRuw20TwEd-Hy-aqc130_provenance
;
np:hasPublicationInfo
dgn-np:NP635109.RA2ycOaGvOmhGFsGxdT-htG6-iOxMRuw20TwEd-Hy-aqc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP635109.RA2ycOaGvOmhGFsGxdT-htG6-iOxMRuw20TwEd-Hy-aqc130_assertion
a
np:Assertion
.
dgn-np:NP635109.RA2ycOaGvOmhGFsGxdT-htG6-iOxMRuw20TwEd-Hy-aqc130_provenance
a
np:Provenance
.
dgn-np:NP635109.RA2ycOaGvOmhGFsGxdT-htG6-iOxMRuw20TwEd-Hy-aqc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP635109.RA2ycOaGvOmhGFsGxdT-htG6-iOxMRuw20TwEd-Hy-aqc130_assertion
{
miriam-gene:2048
a
ncit:C16612
.
lld:C0001080
a
ncit:C7057
.
dgn-gda:DGN2b040cc1565bda8378a62b25dd9277f1
sio:SIO_000628
miriam-gene:2048
,
lld:C0001080
;
a
sio:SIO_001121
.
}
dgn-np:NP635109.RA2ycOaGvOmhGFsGxdT-htG6-iOxMRuw20TwEd-Hy-aqc130_provenance
{
dgn-np:NP635109.RA2ycOaGvOmhGFsGxdT-htG6-iOxMRuw20TwEd-Hy-aqc130_assertion
dcterms:description
"[Our recent studies have indicated that increased Fgfr3 and ERK MAPK signaling in chondrocytes also causes premature synchondrosis closure in the cranial base and vertebrae, accounting for the sometimes fatal stenosis of the foramen magnum and spinal canal in achondroplasia.]. 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:20922792
;
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:NP635109.RA2ycOaGvOmhGFsGxdT-htG6-iOxMRuw20TwEd-Hy-aqc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:23+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" .
}