@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP699530.RAbqlKFtqonUe1S099A0iOOXd9Al6inFZYs3vgCfG868M
> .
@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:NP699530.RAbqlKFtqonUe1S099A0iOOXd9Al6inFZYs3vgCfG868M130_head
{
this:
np:hasAssertion
dgn-np:NP699530.RAbqlKFtqonUe1S099A0iOOXd9Al6inFZYs3vgCfG868M130_assertion
;
np:hasProvenance
dgn-np:NP699530.RAbqlKFtqonUe1S099A0iOOXd9Al6inFZYs3vgCfG868M130_provenance
;
np:hasPublicationInfo
dgn-np:NP699530.RAbqlKFtqonUe1S099A0iOOXd9Al6inFZYs3vgCfG868M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP699530.RAbqlKFtqonUe1S099A0iOOXd9Al6inFZYs3vgCfG868M130_assertion
a
np:Assertion
.
dgn-np:NP699530.RAbqlKFtqonUe1S099A0iOOXd9Al6inFZYs3vgCfG868M130_provenance
a
np:Provenance
.
dgn-np:NP699530.RAbqlKFtqonUe1S099A0iOOXd9Al6inFZYs3vgCfG868M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP699530.RAbqlKFtqonUe1S099A0iOOXd9Al6inFZYs3vgCfG868M130_assertion
{
miriam-gene:2261
a
ncit:C16612
.
lld:C0220658
a
ncit:C7057
.
dgn-gda:DGN9c498db951fe49476c67e5c878962cca
sio:SIO_000628
miriam-gene:2261
,
lld:C0220658
;
a
sio:SIO_001121
.
}
dgn-np:NP699530.RAbqlKFtqonUe1S099A0iOOXd9Al6inFZYs3vgCfG868M130_provenance
{
dgn-np:NP699530.RAbqlKFtqonUe1S099A0iOOXd9Al6inFZYs3vgCfG868M130_assertion
dcterms:description
"[These results together with our earlier observation that achondroplasia results from constitutive activation of the related receptor FGFR3, leads to the prediction that other malformation syndromes attributed to FGFRs, such as Pfeiffer syndrome and Thanatophoric dysplasia, also arise from constitutive receptor activation.]. 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:8755573
;
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:NP699530.RAbqlKFtqonUe1S099A0iOOXd9Al6inFZYs3vgCfG868M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:05+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" .
}