@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP65365.RAKP9likDI0p-1H8U1f7NxpdFcaXGzJZOe1q_VraM2P64
> .
@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/v3.0.0/void/
> .
dgn-np:NP65365.RAKP9likDI0p-1H8U1f7NxpdFcaXGzJZOe1q_VraM2P64130_head
{
this:
np:hasAssertion
dgn-np:NP65365.RAKP9likDI0p-1H8U1f7NxpdFcaXGzJZOe1q_VraM2P64130_assertion
;
np:hasProvenance
dgn-np:NP65365.RAKP9likDI0p-1H8U1f7NxpdFcaXGzJZOe1q_VraM2P64130_provenance
;
np:hasPublicationInfo
dgn-np:NP65365.RAKP9likDI0p-1H8U1f7NxpdFcaXGzJZOe1q_VraM2P64130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP65365.RAKP9likDI0p-1H8U1f7NxpdFcaXGzJZOe1q_VraM2P64130_assertion
a
np:Assertion
.
dgn-np:NP65365.RAKP9likDI0p-1H8U1f7NxpdFcaXGzJZOe1q_VraM2P64130_provenance
a
np:Provenance
.
dgn-np:NP65365.RAKP9likDI0p-1H8U1f7NxpdFcaXGzJZOe1q_VraM2P64130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP65365.RAKP9likDI0p-1H8U1f7NxpdFcaXGzJZOe1q_VraM2P64130_assertion
{
miriam-gene:5925
a
ncit:C16612
.
lld:C0035335
a
ncit:C7057
.
dgn-gda:DGNd68548f7944b360c191f59065b50714e
sio:SIO_000628
miriam-gene:5925
,
lld:C0035335
;
a
sio:SIO_001122
.
}
dgn-np:NP65365.RAKP9likDI0p-1H8U1f7NxpdFcaXGzJZOe1q_VraM2P64130_provenance
{
dgn-np:NP65365.RAKP9likDI0p-1H8U1f7NxpdFcaXGzJZOe1q_VraM2P64130_assertion
dcterms:description
"[Gene testing is indicated in the medical practice of hereditary retinoblastoma for familial risk assessment, while prior counseling is important for an understanding of the risks and benefits of gene testing. With improvements in patient prognosis, counse]. 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:15162822
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP65365.RAKP9likDI0p-1H8U1f7NxpdFcaXGzJZOe1q_VraM2P64130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:15+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}