@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP292476.RAVe9N_a7KClMV_wbsm560TRnpsY-bny5n1i-ZZ8B1V7E
> .
@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#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
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dgn-np:NP292476.RAVe9N_a7KClMV_wbsm560TRnpsY-bny5n1i-ZZ8B1V7E130_assertion
a
np:Assertion
.
dgn-np:NP292476.RAVe9N_a7KClMV_wbsm560TRnpsY-bny5n1i-ZZ8B1V7E130_provenance
a
np:Provenance
.
dgn-np:NP292476.RAVe9N_a7KClMV_wbsm560TRnpsY-bny5n1i-ZZ8B1V7E130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:3651
a
ncit:C16612
.
lld:C0039585
a
ncit:C7057
.
dgn-gda:DGNd1e7692798541a1ea4dc196c01cc977f
sio:SIO_000628
miriam-gene:3651
,
lld:C0039585
;
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.
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dgn-np:NP292476.RAVe9N_a7KClMV_wbsm560TRnpsY-bny5n1i-ZZ8B1V7E130_provenance
{
dgn-np:NP292476.RAVe9N_a7KClMV_wbsm560TRnpsY-bny5n1i-ZZ8B1V7E130_assertion
dcterms:description
"[We discuss in detail findings in GSF from three historical patients with AIS, which include identification of novel mechanisms of AR malfunction, and the potential ability to utilize HCA for personalized treatment of patients affected by this condition.]. 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:20011049
;
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:NP292476.RAVe9N_a7KClMV_wbsm560TRnpsY-bny5n1i-ZZ8B1V7E130_publicationInfo
{
this:
dcterms:created
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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
<
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> , <
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> , <
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
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"v2.1.0" .
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