@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP585833.RAjc_E28UYbzSVorjkbpmwdei9fDViJEjjc8WbAiyECY0
> .
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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
dgn-np:NP585833.RAjc_E28UYbzSVorjkbpmwdei9fDViJEjjc8WbAiyECY0130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP585833.RAjc_E28UYbzSVorjkbpmwdei9fDViJEjjc8WbAiyECY0130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP585833.RAjc_E28UYbzSVorjkbpmwdei9fDViJEjjc8WbAiyECY0130_assertion
a
np:Assertion
.
dgn-np:NP585833.RAjc_E28UYbzSVorjkbpmwdei9fDViJEjjc8WbAiyECY0130_provenance
a
np:Provenance
.
dgn-np:NP585833.RAjc_E28UYbzSVorjkbpmwdei9fDViJEjjc8WbAiyECY0130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:9501
a
ncit:C16612
.
lld:C1140680
a
ncit:C7057
.
dgn-gda:DGN03218bbf5294b8023b6639c952dd03bc
sio:SIO_000628
miriam-gene:9501
,
lld:C1140680
;
a
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.
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dgn-np:NP585833.RAjc_E28UYbzSVorjkbpmwdei9fDViJEjjc8WbAiyECY0130_provenance
{
dgn-np:NP585833.RAjc_E28UYbzSVorjkbpmwdei9fDViJEjjc8WbAiyECY0130_assertion
dcterms:description
"[We determined the exon-intron boundaries of RPH3AL and screened the coding region for mutations by direct sequencing in DNA extracted from 33 tumor samples with allelic loss of 17p13, including 10 medulloblastoma, 14 follicular thyroid cancer (FTC), and 9 ovarian cancer specimens.]. 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:10395805
;
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 .
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dgn-np:NP585833.RAjc_E28UYbzSVorjkbpmwdei9fDViJEjjc8WbAiyECY0130_publicationInfo
{
this:
dcterms:created
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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
<
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> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
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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