@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP781862.RAfwL6tnIorEHGI95n691hsL4r8Oz-GF6nXa77HiBVZnM
> .
@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:NP781862.RAfwL6tnIorEHGI95n691hsL4r8Oz-GF6nXa77HiBVZnM130_head
{
this:
np:hasAssertion
dgn-np:NP781862.RAfwL6tnIorEHGI95n691hsL4r8Oz-GF6nXa77HiBVZnM130_assertion
;
np:hasProvenance
dgn-np:NP781862.RAfwL6tnIorEHGI95n691hsL4r8Oz-GF6nXa77HiBVZnM130_provenance
;
np:hasPublicationInfo
dgn-np:NP781862.RAfwL6tnIorEHGI95n691hsL4r8Oz-GF6nXa77HiBVZnM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP781862.RAfwL6tnIorEHGI95n691hsL4r8Oz-GF6nXa77HiBVZnM130_assertion
a
np:Assertion
.
dgn-np:NP781862.RAfwL6tnIorEHGI95n691hsL4r8Oz-GF6nXa77HiBVZnM130_provenance
a
np:Provenance
.
dgn-np:NP781862.RAfwL6tnIorEHGI95n691hsL4r8Oz-GF6nXa77HiBVZnM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP781862.RAfwL6tnIorEHGI95n691hsL4r8Oz-GF6nXa77HiBVZnM130_assertion
{
miriam-gene:6392
a
ncit:C16612
.
lld:C0027831
a
ncit:C7057
.
dgn-gda:DGNcbe12ef8c91dc31c8940cb347391a2a5
sio:SIO_000628
miriam-gene:6392
,
lld:C0027831
;
a
sio:SIO_001121
.
}
dgn-np:NP781862.RAfwL6tnIorEHGI95n691hsL4r8Oz-GF6nXa77HiBVZnM130_provenance
{
dgn-np:NP781862.RAfwL6tnIorEHGI95n691hsL4r8Oz-GF6nXa77HiBVZnM130_assertion
dcterms:description
"[SDHB protein expression was absent in all 102 phaeochromocytomas and paragangliomas with an SDHB, SDHC, or SDHD mutation, but was present in all 65 paraganglionic tumours related to multiple endocrine neoplasia type 2, von Hippel-Lindau disease, and neurofibromatosis type 1.]. 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:19576851
;
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:NP781862.RAfwL6tnIorEHGI95n691hsL4r8Oz-GF6nXa77HiBVZnM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:53+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" .
}