@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP879109.RAt9Qe2H9p6HoY-khhnPwT3P7s92Nqydfe_S3Bu8odo7A
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP879109.RAt9Qe2H9p6HoY-khhnPwT3P7s92Nqydfe_S3Bu8odo7A130_head
{
this:
np:hasAssertion
dgn-np:NP879109.RAt9Qe2H9p6HoY-khhnPwT3P7s92Nqydfe_S3Bu8odo7A130_assertion
;
np:hasProvenance
dgn-np:NP879109.RAt9Qe2H9p6HoY-khhnPwT3P7s92Nqydfe_S3Bu8odo7A130_provenance
;
np:hasPublicationInfo
dgn-np:NP879109.RAt9Qe2H9p6HoY-khhnPwT3P7s92Nqydfe_S3Bu8odo7A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP879109.RAt9Qe2H9p6HoY-khhnPwT3P7s92Nqydfe_S3Bu8odo7A130_assertion
a
np:Assertion
.
dgn-np:NP879109.RAt9Qe2H9p6HoY-khhnPwT3P7s92Nqydfe_S3Bu8odo7A130_provenance
a
np:Provenance
.
dgn-np:NP879109.RAt9Qe2H9p6HoY-khhnPwT3P7s92Nqydfe_S3Bu8odo7A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP879109.RAt9Qe2H9p6HoY-khhnPwT3P7s92Nqydfe_S3Bu8odo7A130_assertion
{
miriam-gene:2271
a
ncit:C16612
.
lld:C1708350
a
ncit:C7057
.
dgn-gda:DGNfcbbdeedf239596c2f199da3e30aee66
sio:SIO_000628
miriam-gene:2271
,
lld:C1708350
;
a
sio:SIO_001121
.
}
dgn-np:NP879109.RAt9Qe2H9p6HoY-khhnPwT3P7s92Nqydfe_S3Bu8odo7A130_provenance
{
dgn-np:NP879109.RAt9Qe2H9p6HoY-khhnPwT3P7s92Nqydfe_S3Bu8odo7A130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP879109.RAt9Qe2H9p6HoY-khhnPwT3P7s92Nqydfe_S3Bu8odo7A130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:23+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}