@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP262870.RA5wS48HZM-bY9rubNOhFHT7y7xJDBg89Nnv0UKlJZGiQ
> .
@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:NP262870.RA5wS48HZM-bY9rubNOhFHT7y7xJDBg89Nnv0UKlJZGiQ130_head
{
this:
np:hasAssertion
dgn-np:NP262870.RA5wS48HZM-bY9rubNOhFHT7y7xJDBg89Nnv0UKlJZGiQ130_assertion
;
np:hasProvenance
dgn-np:NP262870.RA5wS48HZM-bY9rubNOhFHT7y7xJDBg89Nnv0UKlJZGiQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP262870.RA5wS48HZM-bY9rubNOhFHT7y7xJDBg89Nnv0UKlJZGiQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP262870.RA5wS48HZM-bY9rubNOhFHT7y7xJDBg89Nnv0UKlJZGiQ130_assertion
a
np:Assertion
.
dgn-np:NP262870.RA5wS48HZM-bY9rubNOhFHT7y7xJDBg89Nnv0UKlJZGiQ130_provenance
a
np:Provenance
.
dgn-np:NP262870.RA5wS48HZM-bY9rubNOhFHT7y7xJDBg89Nnv0UKlJZGiQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP262870.RA5wS48HZM-bY9rubNOhFHT7y7xJDBg89Nnv0UKlJZGiQ130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C1832526
a
ncit:C7057
.
dgn-gda:DGNa94fc53393197136d46696cfbd8cbec8
sio:SIO_000628
miriam-gene:5979
,
lld:C1832526
;
a
sio:SIO_001121
.
}
dgn-np:NP262870.RA5wS48HZM-bY9rubNOhFHT7y7xJDBg89Nnv0UKlJZGiQ130_provenance
{
dgn-np:NP262870.RA5wS48HZM-bY9rubNOhFHT7y7xJDBg89Nnv0UKlJZGiQ130_assertion
dcterms:description
"[We conclude that germline RET mutations are predominantly found in bilateral PCC, and that somatic and germline SDHB and SDHD mutations usually occur in sPGL, which has practical consequences for genetic testing algorithms.]. 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:17639058
;
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:NP262870.RA5wS48HZM-bY9rubNOhFHT7y7xJDBg89Nnv0UKlJZGiQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:27+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" .
}