@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP226906.RAAfZar2EkJMIIN-GfInG6bIxWnwuKZopn3_fLNiMZ5i8
> .
@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:NP226906.RAAfZar2EkJMIIN-GfInG6bIxWnwuKZopn3_fLNiMZ5i8130_head
{
this:
np:hasAssertion
dgn-np:NP226906.RAAfZar2EkJMIIN-GfInG6bIxWnwuKZopn3_fLNiMZ5i8130_assertion
;
np:hasProvenance
dgn-np:NP226906.RAAfZar2EkJMIIN-GfInG6bIxWnwuKZopn3_fLNiMZ5i8130_provenance
;
np:hasPublicationInfo
dgn-np:NP226906.RAAfZar2EkJMIIN-GfInG6bIxWnwuKZopn3_fLNiMZ5i8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP226906.RAAfZar2EkJMIIN-GfInG6bIxWnwuKZopn3_fLNiMZ5i8130_assertion
a
np:Assertion
.
dgn-np:NP226906.RAAfZar2EkJMIIN-GfInG6bIxWnwuKZopn3_fLNiMZ5i8130_provenance
a
np:Provenance
.
dgn-np:NP226906.RAAfZar2EkJMIIN-GfInG6bIxWnwuKZopn3_fLNiMZ5i8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP226906.RAAfZar2EkJMIIN-GfInG6bIxWnwuKZopn3_fLNiMZ5i8130_assertion
{
miriam-gene:6794
a
ncit:C16612
.
lld:C0919267
a
ncit:C7057
.
dgn-gda:DGN79fe75156b3b715f2d1862686a405c9a
sio:SIO_000628
miriam-gene:6794
,
lld:C0919267
;
a
sio:SIO_001121
.
}
dgn-np:NP226906.RAAfZar2EkJMIIN-GfInG6bIxWnwuKZopn3_fLNiMZ5i8130_provenance
{
dgn-np:NP226906.RAAfZar2EkJMIIN-GfInG6bIxWnwuKZopn3_fLNiMZ5i8130_assertion
dcterms:description
"[Although somatic mutations of STK11 are reportedly rare in sporadic forms of common cancers linked to PJS, there are no available studies assessing STK11 alterations in larger series of sporadic ovarian tumors with granulosa, Sertoli or combined differentiation.]. 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:15343512
;
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:NP226906.RAAfZar2EkJMIIN-GfInG6bIxWnwuKZopn3_fLNiMZ5i8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:06+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" .
}