@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI
> .
@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:NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI130_head
{
this:
np:hasAssertion
dgn-np:NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI130_assertion
;
np:hasProvenance
dgn-np:NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI130_provenance
;
np:hasPublicationInfo
dgn-np:NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI130_assertion
a
np:Assertion
.
dgn-np:NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI130_provenance
a
np:Provenance
.
dgn-np:NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI130_assertion
{
miriam-gene:2778
a
ncit:C16612
.
lld:C0040136
a
ncit:C7057
.
dgn-gda:DGN795baba59a44dcc3bfd8bd754b5184d0
sio:SIO_000628
miriam-gene:2778
,
lld:C0040136
;
a
sio:SIO_001121
.
}
dgn-np:NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI130_provenance
{
dgn-np:NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI130_assertion
dcterms:description
"[Acquisition of a similar activating mutation in GNAS1 later in life presumably accounts for the restricted distribution of the gsp oncogene, and is associated with the development of isolated lesions (for example, fibrous dysplasia, pituitary or thyroid tumors) without other manifestations of MAS.]. 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:8699958
;
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:NP179399.RADCx1hxoJIX7-HOruFG3hqGtYZzosIOi9Nj6R74nMwmI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:37+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" .
}