@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP555415.RAUKMNAkIivsrQvfyGup9V2rqy8FkdS0JNcK3Y7vN9guU
> .
@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:NP555415.RAUKMNAkIivsrQvfyGup9V2rqy8FkdS0JNcK3Y7vN9guU130_head
{
this:
np:hasAssertion
dgn-np:NP555415.RAUKMNAkIivsrQvfyGup9V2rqy8FkdS0JNcK3Y7vN9guU130_assertion
;
np:hasProvenance
dgn-np:NP555415.RAUKMNAkIivsrQvfyGup9V2rqy8FkdS0JNcK3Y7vN9guU130_provenance
;
np:hasPublicationInfo
dgn-np:NP555415.RAUKMNAkIivsrQvfyGup9V2rqy8FkdS0JNcK3Y7vN9guU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP555415.RAUKMNAkIivsrQvfyGup9V2rqy8FkdS0JNcK3Y7vN9guU130_assertion
a
np:Assertion
.
dgn-np:NP555415.RAUKMNAkIivsrQvfyGup9V2rqy8FkdS0JNcK3Y7vN9guU130_provenance
a
np:Provenance
.
dgn-np:NP555415.RAUKMNAkIivsrQvfyGup9V2rqy8FkdS0JNcK3Y7vN9guU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP555415.RAUKMNAkIivsrQvfyGup9V2rqy8FkdS0JNcK3Y7vN9guU130_assertion
{
miriam-gene:4880
a
ncit:C16612
.
lld:C0001080
a
ncit:C7057
.
dgn-gda:DGNc2cfadf770b4784446eead60563f911b
sio:SIO_000628
miriam-gene:4880
,
lld:C0001080
;
a
sio:SIO_001121
.
}
dgn-np:NP555415.RAUKMNAkIivsrQvfyGup9V2rqy8FkdS0JNcK3Y7vN9guU130_provenance
{
dgn-np:NP555415.RAUKMNAkIivsrQvfyGup9V2rqy8FkdS0JNcK3Y7vN9guU130_assertion
dcterms:description
"[We have shown that targeted overexpression of CNP in cartilage or systemic administration of CNP reverses the impaired skeletal growth of mice model of achondroplasia, the most common form of human skeletal dysplasias.]. 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:20567091
;
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:NP555415.RAUKMNAkIivsrQvfyGup9V2rqy8FkdS0JNcK3Y7vN9guU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:35+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" .
}