@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP421935.RAwrlD53Fguo5cSFqu_pbiQSgZZUq5fME96YhRnkdyE7Y
> .
@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:NP421935.RAwrlD53Fguo5cSFqu_pbiQSgZZUq5fME96YhRnkdyE7Y130_head
{
this:
np:hasAssertion
dgn-np:NP421935.RAwrlD53Fguo5cSFqu_pbiQSgZZUq5fME96YhRnkdyE7Y130_assertion
;
np:hasProvenance
dgn-np:NP421935.RAwrlD53Fguo5cSFqu_pbiQSgZZUq5fME96YhRnkdyE7Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP421935.RAwrlD53Fguo5cSFqu_pbiQSgZZUq5fME96YhRnkdyE7Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP421935.RAwrlD53Fguo5cSFqu_pbiQSgZZUq5fME96YhRnkdyE7Y130_assertion
a
np:Assertion
.
dgn-np:NP421935.RAwrlD53Fguo5cSFqu_pbiQSgZZUq5fME96YhRnkdyE7Y130_provenance
a
np:Provenance
.
dgn-np:NP421935.RAwrlD53Fguo5cSFqu_pbiQSgZZUq5fME96YhRnkdyE7Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP421935.RAwrlD53Fguo5cSFqu_pbiQSgZZUq5fME96YhRnkdyE7Y130_assertion
{
miriam-gene:2271
a
ncit:C16612
.
lld:C3160732
a
ncit:C7057
.
dgn-gda:DGN64497d0ff000c8ed09bbdda6882c5dc3
sio:SIO_000628
miriam-gene:2271
,
lld:C3160732
;
a
sio:SIO_001121
.
}
dgn-np:NP421935.RAwrlD53Fguo5cSFqu_pbiQSgZZUq5fME96YhRnkdyE7Y130_provenance
{
dgn-np:NP421935.RAwrlD53Fguo5cSFqu_pbiQSgZZUq5fME96YhRnkdyE7Y130_assertion
dcterms:description
"[Hereditary leiomyomatosis renal cell carcinoma (HLRCC) is an aggressive form of RCC characterized by germline mutation of the Krebs cycle enzyme fumarate hydratase (FH), and one known to be highly metastatic and unusually lethal.]. 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:19963135
;
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:NP421935.RAwrlD53Fguo5cSFqu_pbiQSgZZUq5fME96YhRnkdyE7Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:10+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" .
}