@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP646117.RA9QZS9OJPcBM1EoOCm8sVMml3mEjxuq6tCnHp-7ChRhE
> .
@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:NP646117.RA9QZS9OJPcBM1EoOCm8sVMml3mEjxuq6tCnHp-7ChRhE130_head
{
this:
np:hasAssertion
dgn-np:NP646117.RA9QZS9OJPcBM1EoOCm8sVMml3mEjxuq6tCnHp-7ChRhE130_assertion
;
np:hasProvenance
dgn-np:NP646117.RA9QZS9OJPcBM1EoOCm8sVMml3mEjxuq6tCnHp-7ChRhE130_provenance
;
np:hasPublicationInfo
dgn-np:NP646117.RA9QZS9OJPcBM1EoOCm8sVMml3mEjxuq6tCnHp-7ChRhE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP646117.RA9QZS9OJPcBM1EoOCm8sVMml3mEjxuq6tCnHp-7ChRhE130_assertion
a
np:Assertion
.
dgn-np:NP646117.RA9QZS9OJPcBM1EoOCm8sVMml3mEjxuq6tCnHp-7ChRhE130_provenance
a
np:Provenance
.
dgn-np:NP646117.RA9QZS9OJPcBM1EoOCm8sVMml3mEjxuq6tCnHp-7ChRhE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP646117.RA9QZS9OJPcBM1EoOCm8sVMml3mEjxuq6tCnHp-7ChRhE130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0027708
a
ncit:C7057
.
dgn-gda:DGN1f2a50c6e708aa169f83d673f2819f37
sio:SIO_000628
miriam-gene:5979
,
lld:C0027708
;
a
sio:SIO_001121
.
}
dgn-np:NP646117.RA9QZS9OJPcBM1EoOCm8sVMml3mEjxuq6tCnHp-7ChRhE130_provenance
{
dgn-np:NP646117.RA9QZS9OJPcBM1EoOCm8sVMml3mEjxuq6tCnHp-7ChRhE130_assertion
dcterms:description
"[Although this limited evaluation failed to show abnormalities, we speculate that comprehensive analysis of the RET gene may identify mutations to account for the development of WT in this and other children with WT.]. 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:18090939
;
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:NP646117.RA9QZS9OJPcBM1EoOCm8sVMml3mEjxuq6tCnHp-7ChRhE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:38+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" .
}