@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP472096.RAropMS2EJ9kDpqIKdCkd5CwIeyh8r_9eDertsXhF9gAk
> .
@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:NP472096.RAropMS2EJ9kDpqIKdCkd5CwIeyh8r_9eDertsXhF9gAk130_head
{
this:
np:hasAssertion
dgn-np:NP472096.RAropMS2EJ9kDpqIKdCkd5CwIeyh8r_9eDertsXhF9gAk130_assertion
;
np:hasProvenance
dgn-np:NP472096.RAropMS2EJ9kDpqIKdCkd5CwIeyh8r_9eDertsXhF9gAk130_provenance
;
np:hasPublicationInfo
dgn-np:NP472096.RAropMS2EJ9kDpqIKdCkd5CwIeyh8r_9eDertsXhF9gAk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP472096.RAropMS2EJ9kDpqIKdCkd5CwIeyh8r_9eDertsXhF9gAk130_assertion
a
np:Assertion
.
dgn-np:NP472096.RAropMS2EJ9kDpqIKdCkd5CwIeyh8r_9eDertsXhF9gAk130_provenance
a
np:Provenance
.
dgn-np:NP472096.RAropMS2EJ9kDpqIKdCkd5CwIeyh8r_9eDertsXhF9gAk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP472096.RAropMS2EJ9kDpqIKdCkd5CwIeyh8r_9eDertsXhF9gAk130_assertion
{
miriam-gene:80347
a
ncit:C16612
.
lld:C0014130
a
ncit:C7057
.
dgn-gda:DGN6258806d049674181bf0b71af343f8d5
sio:SIO_000628
miriam-gene:80347
,
lld:C0014130
;
a
sio:SIO_001121
.
}
dgn-np:NP472096.RAropMS2EJ9kDpqIKdCkd5CwIeyh8r_9eDertsXhF9gAk130_provenance
{
dgn-np:NP472096.RAropMS2EJ9kDpqIKdCkd5CwIeyh8r_9eDertsXhF9gAk130_assertion
dcterms:description
"[Although deficient Gs activity appears to play an important role in the pathogenesis of these disorders, it is possible that Gs deficiency must be combined with other factors that limit cAMP production to cause clinically overt endocrine disease.]. 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:3003142
;
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:NP472096.RAropMS2EJ9kDpqIKdCkd5CwIeyh8r_9eDertsXhF9gAk130_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" .
}