@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP327219.RAaY2FJvSMHQwFodk_nOXyv5g8i8GWTMyex_dz16QM8WI
> .
@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:NP327219.RAaY2FJvSMHQwFodk_nOXyv5g8i8GWTMyex_dz16QM8WI130_head
{
this:
np:hasAssertion
dgn-np:NP327219.RAaY2FJvSMHQwFodk_nOXyv5g8i8GWTMyex_dz16QM8WI130_assertion
;
np:hasProvenance
dgn-np:NP327219.RAaY2FJvSMHQwFodk_nOXyv5g8i8GWTMyex_dz16QM8WI130_provenance
;
np:hasPublicationInfo
dgn-np:NP327219.RAaY2FJvSMHQwFodk_nOXyv5g8i8GWTMyex_dz16QM8WI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP327219.RAaY2FJvSMHQwFodk_nOXyv5g8i8GWTMyex_dz16QM8WI130_assertion
a
np:Assertion
.
dgn-np:NP327219.RAaY2FJvSMHQwFodk_nOXyv5g8i8GWTMyex_dz16QM8WI130_provenance
a
np:Provenance
.
dgn-np:NP327219.RAaY2FJvSMHQwFodk_nOXyv5g8i8GWTMyex_dz16QM8WI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP327219.RAaY2FJvSMHQwFodk_nOXyv5g8i8GWTMyex_dz16QM8WI130_assertion
{
miriam-gene:6392
a
ncit:C16612
.
lld:C0019562
a
ncit:C7057
.
dgn-gda:DGNa4c7eb6d9deafa43b27b0d8aa61858b3
sio:SIO_000628
miriam-gene:6392
,
lld:C0019562
;
a
sio:SIO_001121
.
}
dgn-np:NP327219.RAaY2FJvSMHQwFodk_nOXyv5g8i8GWTMyex_dz16QM8WI130_provenance
{
dgn-np:NP327219.RAaY2FJvSMHQwFodk_nOXyv5g8i8GWTMyex_dz16QM8WI130_assertion
dcterms:description
"[In addition to mutations in RET and VHL in familial disease, germline mutations in SDHD and SDHB genes that encode subunits of mitochondrial complex II have also been associated with the development of familial phaeochromocytomas.]. 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:12618761
;
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:NP327219.RAaY2FJvSMHQwFodk_nOXyv5g8i8GWTMyex_dz16QM8WI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:11+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" .
}