@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP613434.RAbg1Aa0ge4rxKfDYRCLC-CCLILP8yr2A0B26FuWmyLTI
> .
@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:NP613434.RAbg1Aa0ge4rxKfDYRCLC-CCLILP8yr2A0B26FuWmyLTI130_head
{
this:
np:hasAssertion
dgn-np:NP613434.RAbg1Aa0ge4rxKfDYRCLC-CCLILP8yr2A0B26FuWmyLTI130_assertion
;
np:hasProvenance
dgn-np:NP613434.RAbg1Aa0ge4rxKfDYRCLC-CCLILP8yr2A0B26FuWmyLTI130_provenance
;
np:hasPublicationInfo
dgn-np:NP613434.RAbg1Aa0ge4rxKfDYRCLC-CCLILP8yr2A0B26FuWmyLTI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP613434.RAbg1Aa0ge4rxKfDYRCLC-CCLILP8yr2A0B26FuWmyLTI130_assertion
a
np:Assertion
.
dgn-np:NP613434.RAbg1Aa0ge4rxKfDYRCLC-CCLILP8yr2A0B26FuWmyLTI130_provenance
a
np:Provenance
.
dgn-np:NP613434.RAbg1Aa0ge4rxKfDYRCLC-CCLILP8yr2A0B26FuWmyLTI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP613434.RAbg1Aa0ge4rxKfDYRCLC-CCLILP8yr2A0B26FuWmyLTI130_assertion
{
miriam-gene:6392
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNf858527ebf15db7a618b5c7b9ab2f8bb
sio:SIO_000628
miriam-gene:6392
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP613434.RAbg1Aa0ge4rxKfDYRCLC-CCLILP8yr2A0B26FuWmyLTI130_provenance
{
dgn-np:NP613434.RAbg1Aa0ge4rxKfDYRCLC-CCLILP8yr2A0B26FuWmyLTI130_assertion
dcterms:description
"[Despite the very recent discovery that about 25% of apparently sporadic forms of pheochromocytoma are actually due to germline mutations of RET, VHL, SDHB or SDHD genes, the genetic bases of the tumourigenesis of this type of cancer are still incompletely understood.]. 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:14974911
;
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:NP613434.RAbg1Aa0ge4rxKfDYRCLC-CCLILP8yr2A0B26FuWmyLTI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:11+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" .
}