@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP820907.RAmAr8b4do1xr1Zkd91YYYk23fCM7ymDI9fI24-_3Dr9k
> .
@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:NP820907.RAmAr8b4do1xr1Zkd91YYYk23fCM7ymDI9fI24-_3Dr9k130_head
{
this:
np:hasAssertion
dgn-np:NP820907.RAmAr8b4do1xr1Zkd91YYYk23fCM7ymDI9fI24-_3Dr9k130_assertion
;
np:hasProvenance
dgn-np:NP820907.RAmAr8b4do1xr1Zkd91YYYk23fCM7ymDI9fI24-_3Dr9k130_provenance
;
np:hasPublicationInfo
dgn-np:NP820907.RAmAr8b4do1xr1Zkd91YYYk23fCM7ymDI9fI24-_3Dr9k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP820907.RAmAr8b4do1xr1Zkd91YYYk23fCM7ymDI9fI24-_3Dr9k130_assertion
a
np:Assertion
.
dgn-np:NP820907.RAmAr8b4do1xr1Zkd91YYYk23fCM7ymDI9fI24-_3Dr9k130_provenance
a
np:Provenance
.
dgn-np:NP820907.RAmAr8b4do1xr1Zkd91YYYk23fCM7ymDI9fI24-_3Dr9k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP820907.RAmAr8b4do1xr1Zkd91YYYk23fCM7ymDI9fI24-_3Dr9k130_assertion
{
miriam-gene:3081
a
ncit:C16612
.
lld:C0267375
a
ncit:C7057
.
dgn-gda:DGNeae5013cf4b06ee146e68a69f4bd120c
sio:SIO_000628
miriam-gene:3081
,
lld:C0267375
;
a
sio:SIO_001121
.
}
dgn-np:NP820907.RAmAr8b4do1xr1Zkd91YYYk23fCM7ymDI9fI24-_3Dr9k130_provenance
{
dgn-np:NP820907.RAmAr8b4do1xr1Zkd91YYYk23fCM7ymDI9fI24-_3Dr9k130_assertion
dcterms:description
"[More frequent involvement of the VHL gene in PD and surrounding CC and involvement of p53 in HGD and CC in FD may represent genetic differences between the development of PD and FD and may be the cause of the different morphology.]. 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:9744312
;
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:NP820907.RAmAr8b4do1xr1Zkd91YYYk23fCM7ymDI9fI24-_3Dr9k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:23+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" .
}