@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP689182.RADO3sSvPd_KPJUG0Vj6yvSJvW4RDRYhMjIeHkcvGGmvE
> .
@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/v3.0.0/void/
> .
dgn-np:NP689182.RADO3sSvPd_KPJUG0Vj6yvSJvW4RDRYhMjIeHkcvGGmvE130_head
{
this:
np:hasAssertion
dgn-np:NP689182.RADO3sSvPd_KPJUG0Vj6yvSJvW4RDRYhMjIeHkcvGGmvE130_assertion
;
np:hasProvenance
dgn-np:NP689182.RADO3sSvPd_KPJUG0Vj6yvSJvW4RDRYhMjIeHkcvGGmvE130_provenance
;
np:hasPublicationInfo
dgn-np:NP689182.RADO3sSvPd_KPJUG0Vj6yvSJvW4RDRYhMjIeHkcvGGmvE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP689182.RADO3sSvPd_KPJUG0Vj6yvSJvW4RDRYhMjIeHkcvGGmvE130_assertion
a
np:Assertion
.
dgn-np:NP689182.RADO3sSvPd_KPJUG0Vj6yvSJvW4RDRYhMjIeHkcvGGmvE130_provenance
a
np:Provenance
.
dgn-np:NP689182.RADO3sSvPd_KPJUG0Vj6yvSJvW4RDRYhMjIeHkcvGGmvE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP689182.RADO3sSvPd_KPJUG0Vj6yvSJvW4RDRYhMjIeHkcvGGmvE130_assertion
{
miriam-gene:6392
a
ncit:C16612
.
lld:C0596263
a
ncit:C7057
.
dgn-gda:DGN490eb91b0511402df7cb8c6819353880
sio:SIO_000628
miriam-gene:6392
,
lld:C0596263
;
a
sio:SIO_001122
.
}
dgn-np:NP689182.RADO3sSvPd_KPJUG0Vj6yvSJvW4RDRYhMjIeHkcvGGmvE130_provenance
{
dgn-np:NP689182.RADO3sSvPd_KPJUG0Vj6yvSJvW4RDRYhMjIeHkcvGGmvE130_assertion
dcterms:description
"[Thus, PGL caused by SDHD mutations represents an unusual example of an inherited monogenic tumor syndrome because the risk of tumorigenesis shows an absolute dependence on the sex of the transmitting parent and may be modified by a ubiquitous environmental factor.]. 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:15264276
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP689182.RADO3sSvPd_KPJUG0Vj6yvSJvW4RDRYhMjIeHkcvGGmvE130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:44:35+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}