@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP731261.RAB38AyMaV1xA2TPEke51aLGmvAjGBXIj3MQ9S_np7Cjs
> .
@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:NP731261.RAB38AyMaV1xA2TPEke51aLGmvAjGBXIj3MQ9S_np7Cjs130_head
{
this:
np:hasAssertion
dgn-np:NP731261.RAB38AyMaV1xA2TPEke51aLGmvAjGBXIj3MQ9S_np7Cjs130_assertion
;
np:hasProvenance
dgn-np:NP731261.RAB38AyMaV1xA2TPEke51aLGmvAjGBXIj3MQ9S_np7Cjs130_provenance
;
np:hasPublicationInfo
dgn-np:NP731261.RAB38AyMaV1xA2TPEke51aLGmvAjGBXIj3MQ9S_np7Cjs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP731261.RAB38AyMaV1xA2TPEke51aLGmvAjGBXIj3MQ9S_np7Cjs130_assertion
a
np:Assertion
.
dgn-np:NP731261.RAB38AyMaV1xA2TPEke51aLGmvAjGBXIj3MQ9S_np7Cjs130_provenance
a
np:Provenance
.
dgn-np:NP731261.RAB38AyMaV1xA2TPEke51aLGmvAjGBXIj3MQ9S_np7Cjs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP731261.RAB38AyMaV1xA2TPEke51aLGmvAjGBXIj3MQ9S_np7Cjs130_assertion
{
miriam-gene:325
a
ncit:C16612
.
lld:C0343284
a
ncit:C7057
.
dgn-gda:DGN0d0ca027a38a5e807fd2c41e36d6da2d
sio:SIO_000628
miriam-gene:325
,
lld:C0343284
;
a
sio:SIO_001121
.
}
dgn-np:NP731261.RAB38AyMaV1xA2TPEke51aLGmvAjGBXIj3MQ9S_np7Cjs130_provenance
{
dgn-np:NP731261.RAB38AyMaV1xA2TPEke51aLGmvAjGBXIj3MQ9S_np7Cjs130_assertion
dcterms:description
"[To elucidate whether systemic administration of CNP would be a novel medical treatment for chondrodysplasias, for which no drug therapy has yet been developed, we investigated the effect of circulating CNP by using the CNP transgenic mice with an increased circulating CNP under the control of human serum amyloid P component promoter (SAP-Nppc-Tg mice).]. 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:20610569
;
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:NP731261.RAB38AyMaV1xA2TPEke51aLGmvAjGBXIj3MQ9S_np7Cjs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:23+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" .
}