@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8
> .
@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:NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8130_head
{
this:
np:hasAssertion
dgn-np:NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8130_assertion
;
np:hasProvenance
dgn-np:NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8130_provenance
;
np:hasPublicationInfo
dgn-np:NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8130_assertion
a
np:Assertion
.
dgn-np:NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8130_provenance
a
np:Provenance
.
dgn-np:NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8130_assertion
{
miriam-gene:2271
a
ncit:C16612
.
lld:C0022665
a
ncit:C7057
.
dgn-gda:DGNaf6bd7e63f250d7d97d58796ac1f5490
sio:SIO_000628
miriam-gene:2271
,
lld:C0022665
;
a
sio:SIO_001121
.
}
dgn-np:NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8130_provenance
{
dgn-np:NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8130_assertion
dcterms:description
"[Due to the incomplete penetrance of HLRCC, the authors propose to extend the FH mutation analysis to every patient with PRCCII occurring before 40 years of age or when renal tumour harbours characteristic histologic features, in order to discover previously ignored HLRCC affected families.]. 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:21398687
;
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:NP622500.RAE7SH13FV0dTyaIog-BAH-spCeluXTc9HF2HxWKCIGd8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:16+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" .
}