@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP707457.RAgfqc6jKXbbiGiXp5H-XYf84SnllOpRwmfcGvlvejBKk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP707457.RAgfqc6jKXbbiGiXp5H-XYf84SnllOpRwmfcGvlvejBKk130_head
{
this:
np:hasAssertion
dgn-np:NP707457.RAgfqc6jKXbbiGiXp5H-XYf84SnllOpRwmfcGvlvejBKk130_assertion
;
np:hasProvenance
dgn-np:NP707457.RAgfqc6jKXbbiGiXp5H-XYf84SnllOpRwmfcGvlvejBKk130_provenance
;
np:hasPublicationInfo
dgn-np:NP707457.RAgfqc6jKXbbiGiXp5H-XYf84SnllOpRwmfcGvlvejBKk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP707457.RAgfqc6jKXbbiGiXp5H-XYf84SnllOpRwmfcGvlvejBKk130_assertion
a
np:Assertion
.
dgn-np:NP707457.RAgfqc6jKXbbiGiXp5H-XYf84SnllOpRwmfcGvlvejBKk130_provenance
a
np:Provenance
.
dgn-np:NP707457.RAgfqc6jKXbbiGiXp5H-XYf84SnllOpRwmfcGvlvejBKk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP707457.RAgfqc6jKXbbiGiXp5H-XYf84SnllOpRwmfcGvlvejBKk130_assertion
{
miriam-gene:4221
a
ncit:C16612
.
lld:C0032019
a
ncit:C7057
.
dgn-gda:DGN32a3e6100014b653feeccb1f620e9cb9
sio:SIO_000628
miriam-gene:4221
,
lld:C0032019
;
a
sio:SIO_001121
.
}
dgn-np:NP707457.RAgfqc6jKXbbiGiXp5H-XYf84SnllOpRwmfcGvlvejBKk130_provenance
{
dgn-np:NP707457.RAgfqc6jKXbbiGiXp5H-XYf84SnllOpRwmfcGvlvejBKk130_assertion
dcterms:description
"[Similarly, there is little evidence to suggest that the mutations involved in genetic syndromes associated with pituitary tumors (such as the gsp, MEN1, PKAR1A or AIP mutations) are common in sporadic tumors.]. 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:19058014
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP707457.RAgfqc6jKXbbiGiXp5H-XYf84SnllOpRwmfcGvlvejBKk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:05+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}