@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP707458.RAaWTYS-dVOtZXv1eHL23r5qB2qvTv7qZipR_PePh1ZY8
> .
@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:NP707458.RAaWTYS-dVOtZXv1eHL23r5qB2qvTv7qZipR_PePh1ZY8130_head
{
this:
np:hasAssertion
dgn-np:NP707458.RAaWTYS-dVOtZXv1eHL23r5qB2qvTv7qZipR_PePh1ZY8130_assertion
;
np:hasProvenance
dgn-np:NP707458.RAaWTYS-dVOtZXv1eHL23r5qB2qvTv7qZipR_PePh1ZY8130_provenance
;
np:hasPublicationInfo
dgn-np:NP707458.RAaWTYS-dVOtZXv1eHL23r5qB2qvTv7qZipR_PePh1ZY8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP707458.RAaWTYS-dVOtZXv1eHL23r5qB2qvTv7qZipR_PePh1ZY8130_assertion
a
np:Assertion
.
dgn-np:NP707458.RAaWTYS-dVOtZXv1eHL23r5qB2qvTv7qZipR_PePh1ZY8130_provenance
a
np:Provenance
.
dgn-np:NP707458.RAaWTYS-dVOtZXv1eHL23r5qB2qvTv7qZipR_PePh1ZY8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP707458.RAaWTYS-dVOtZXv1eHL23r5qB2qvTv7qZipR_PePh1ZY8130_assertion
{
miriam-gene:54998
a
ncit:C16612
.
lld:C0032019
a
ncit:C7057
.
dgn-gda:DGN1c700a92c1f99f0bd4e35454222de8c9
sio:SIO_000628
miriam-gene:54998
,
lld:C0032019
;
a
sio:SIO_001121
.
}
dgn-np:NP707458.RAaWTYS-dVOtZXv1eHL23r5qB2qvTv7qZipR_PePh1ZY8130_provenance
{
dgn-np:NP707458.RAaWTYS-dVOtZXv1eHL23r5qB2qvTv7qZipR_PePh1ZY8130_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:NP707458.RAaWTYS-dVOtZXv1eHL23r5qB2qvTv7qZipR_PePh1ZY8130_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" .
}