@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP578762.RAA9XPqXAoAcb5P3xP67gde5c6sphPyFReWMFg70ZJYUA
> .
@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:NP578762.RAA9XPqXAoAcb5P3xP67gde5c6sphPyFReWMFg70ZJYUA130_head
{
this:
np:hasAssertion
dgn-np:NP578762.RAA9XPqXAoAcb5P3xP67gde5c6sphPyFReWMFg70ZJYUA130_assertion
;
np:hasProvenance
dgn-np:NP578762.RAA9XPqXAoAcb5P3xP67gde5c6sphPyFReWMFg70ZJYUA130_provenance
;
np:hasPublicationInfo
dgn-np:NP578762.RAA9XPqXAoAcb5P3xP67gde5c6sphPyFReWMFg70ZJYUA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP578762.RAA9XPqXAoAcb5P3xP67gde5c6sphPyFReWMFg70ZJYUA130_assertion
a
np:Assertion
.
dgn-np:NP578762.RAA9XPqXAoAcb5P3xP67gde5c6sphPyFReWMFg70ZJYUA130_provenance
a
np:Provenance
.
dgn-np:NP578762.RAA9XPqXAoAcb5P3xP67gde5c6sphPyFReWMFg70ZJYUA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP578762.RAA9XPqXAoAcb5P3xP67gde5c6sphPyFReWMFg70ZJYUA130_assertion
{
miriam-gene:4158
a
ncit:C16612
.
lld:C0037769
a
ncit:C7057
.
dgn-gda:DGNbcda7978c286863e70c51f25cc5e705c
sio:SIO_000628
miriam-gene:4158
,
lld:C0037769
;
a
sio:SIO_001121
.
}
dgn-np:NP578762.RAA9XPqXAoAcb5P3xP67gde5c6sphPyFReWMFg70ZJYUA130_provenance
{
dgn-np:NP578762.RAA9XPqXAoAcb5P3xP67gde5c6sphPyFReWMFg70ZJYUA130_assertion
dcterms:description
"[The results showed that the haplotype TCCT in MC2R promoter significantly led to increased MC2R expression and strong responses to ACTH, providing evidence of the molecular mechanism of ACTH therapy in IS.]. 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:20042918
;
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:NP578762.RAA9XPqXAoAcb5P3xP67gde5c6sphPyFReWMFg70ZJYUA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:49+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" .
}