@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP472217.RAIGKik3VtJK4DXgpUpPDqWAqS6K4lxXWt0M3rA7Z3pIQ
> .
@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:NP472217.RAIGKik3VtJK4DXgpUpPDqWAqS6K4lxXWt0M3rA7Z3pIQ130_head
{
this:
np:hasAssertion
dgn-np:NP472217.RAIGKik3VtJK4DXgpUpPDqWAqS6K4lxXWt0M3rA7Z3pIQ130_assertion
;
np:hasProvenance
dgn-np:NP472217.RAIGKik3VtJK4DXgpUpPDqWAqS6K4lxXWt0M3rA7Z3pIQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP472217.RAIGKik3VtJK4DXgpUpPDqWAqS6K4lxXWt0M3rA7Z3pIQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP472217.RAIGKik3VtJK4DXgpUpPDqWAqS6K4lxXWt0M3rA7Z3pIQ130_assertion
a
np:Assertion
.
dgn-np:NP472217.RAIGKik3VtJK4DXgpUpPDqWAqS6K4lxXWt0M3rA7Z3pIQ130_provenance
a
np:Provenance
.
dgn-np:NP472217.RAIGKik3VtJK4DXgpUpPDqWAqS6K4lxXWt0M3rA7Z3pIQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP472217.RAIGKik3VtJK4DXgpUpPDqWAqS6K4lxXWt0M3rA7Z3pIQ130_assertion
{
miriam-gene:4306
a
ncit:C16612
.
lld:C0268436
a
ncit:C7057
.
dgn-gda:DGN0d0a994025ec4844cf51660b65d8cfb0
sio:SIO_000628
miriam-gene:4306
,
lld:C0268436
;
a
sio:SIO_001121
.
}
dgn-np:NP472217.RAIGKik3VtJK4DXgpUpPDqWAqS6K4lxXWt0M3rA7Z3pIQ130_provenance
{
dgn-np:NP472217.RAIGKik3VtJK4DXgpUpPDqWAqS6K4lxXWt0M3rA7Z3pIQ130_assertion
dcterms:description
"[Molecular analysis of the NR3C2 gene in PHA1 patients is warranted to detect novel mutations in order to clarify the underlying genetic cause, which may extend the insight into relevant functional regions of the hMR protein.]. 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:17287415
;
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:NP472217.RAIGKik3VtJK4DXgpUpPDqWAqS6K4lxXWt0M3rA7Z3pIQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:43+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" .
}