@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP655384.RA8kplLSNUTAM8dc_PNN-698NhgQO7ES7X34S5DyhNNCE
> .
@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#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP655384.RA8kplLSNUTAM8dc_PNN-698NhgQO7ES7X34S5DyhNNCE130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP655384.RA8kplLSNUTAM8dc_PNN-698NhgQO7ES7X34S5DyhNNCE130_assertion
a
np:Assertion
.
dgn-np:NP655384.RA8kplLSNUTAM8dc_PNN-698NhgQO7ES7X34S5DyhNNCE130_provenance
a
np:Provenance
.
dgn-np:NP655384.RA8kplLSNUTAM8dc_PNN-698NhgQO7ES7X34S5DyhNNCE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP655384.RA8kplLSNUTAM8dc_PNN-698NhgQO7ES7X34S5DyhNNCE130_assertion
{
miriam-gene:6392
a
ncit:C16612
.
lld:C0019562
a
ncit:C7057
.
dgn-gda:DGN282b005c5c2e0eff9496727622d6b981
sio:SIO_000628
miriam-gene:6392
,
lld:C0019562
;
a
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.
}
dgn-np:NP655384.RA8kplLSNUTAM8dc_PNN-698NhgQO7ES7X34S5DyhNNCE130_provenance
{
dgn-np:NP655384.RA8kplLSNUTAM8dc_PNN-698NhgQO7ES7X34S5DyhNNCE130_assertion
dcterms:description
"[We suggest that sequential mutation analysis should be directed first at RET, followed by VHL and SDHD for patients with bilateral adrenal PCC at diagnosis, and at SDHB and SDHD for patients with sPGL.]. 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:17639058
;
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:NP655384.RA8kplLSNUTAM8dc_PNN-698NhgQO7ES7X34S5DyhNNCE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:34+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
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pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
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> , <
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
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"v2.1.0" .
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