@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP166530.RAO1ZcK_2xvJlzVwrQGSnA8kbnKKrGrb__rRVQxjSSIGU
> .
@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:NP166530.RAO1ZcK_2xvJlzVwrQGSnA8kbnKKrGrb__rRVQxjSSIGU130_head
{
this:
np:hasAssertion
dgn-np:NP166530.RAO1ZcK_2xvJlzVwrQGSnA8kbnKKrGrb__rRVQxjSSIGU130_assertion
;
np:hasProvenance
dgn-np:NP166530.RAO1ZcK_2xvJlzVwrQGSnA8kbnKKrGrb__rRVQxjSSIGU130_provenance
;
np:hasPublicationInfo
dgn-np:NP166530.RAO1ZcK_2xvJlzVwrQGSnA8kbnKKrGrb__rRVQxjSSIGU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP166530.RAO1ZcK_2xvJlzVwrQGSnA8kbnKKrGrb__rRVQxjSSIGU130_assertion
a
np:Assertion
.
dgn-np:NP166530.RAO1ZcK_2xvJlzVwrQGSnA8kbnKKrGrb__rRVQxjSSIGU130_provenance
a
np:Provenance
.
dgn-np:NP166530.RAO1ZcK_2xvJlzVwrQGSnA8kbnKKrGrb__rRVQxjSSIGU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP166530.RAO1ZcK_2xvJlzVwrQGSnA8kbnKKrGrb__rRVQxjSSIGU130_assertion
{
miriam-gene:846
a
ncit:C16612
.
lld:C0178874
a
ncit:C7057
.
dgn-gda:DGN8d64b88f6288922eb8220f848654bd7c
sio:SIO_000628
miriam-gene:846
,
lld:C0178874
;
a
sio:SIO_001121
.
}
dgn-np:NP166530.RAO1ZcK_2xvJlzVwrQGSnA8kbnKKrGrb__rRVQxjSSIGU130_provenance
{
dgn-np:NP166530.RAO1ZcK_2xvJlzVwrQGSnA8kbnKKrGrb__rRVQxjSSIGU130_assertion
dcterms:description
"[Although mutation of the CaR does not appear to be an early event in carcinogenesis, loss or upregulation of normal CaR function can contribute to several aspects of neoplastic progression, so that therapeutic strategies directed at the CaR could potentially serve a supportive function in cancer management.]. 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:15200153
;
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:NP166530.RAO1ZcK_2xvJlzVwrQGSnA8kbnKKrGrb__rRVQxjSSIGU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:30+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" .
}