@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg
> .
@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 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:NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg130_head
{
this:
np:hasAssertion
dgn-np:NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg130_assertion
;
np:hasProvenance
dgn-np:NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg130_provenance
;
np:hasPublicationInfo
dgn-np:NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg130_assertion
a
np:Assertion
.
dgn-np:NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg130_provenance
a
np:Provenance
.
dgn-np:NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg130_assertion
{
miriam-gene:23560
a
ncit:C16612
.
lld:C0040136
a
ncit:C7057
.
dgn-gda:DGNd7a9b6c872ace969121d6cb888455599
sio:SIO_000628
miriam-gene:23560
,
lld:C0040136
;
a
sio:SIO_001121
.
}
dgn-np:NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg130_provenance
{
dgn-np:NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg130_assertion
dct:description
"[The postulated proto-oncogenic character of the gene encoding the alpha sub-unit of the stimulatory GTP-binding protein Gs alpha (gsp) in pituitary and thyroid tumors, the finding of identical somatic gsp mutations in the myocardium of patients with McCune-Albright syndrome, and the associated endocrine anomalies of the Carney complex prompted us to investigate the occurrence of activating missense mutations in the Gs alpha gene in 10 sporadically occurring atrial myxomas and in 8 tumors from 7 patients with Carney complex.]. 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:8698339
;
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:NP937042.RAObd6QuEELliaxNpRue-LVAWHvEt3CvfBxcL4deDKZWg130_publicationInfo
{
this:
dct:created
"2014-10-02T12:41:34+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct: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" .
}