@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP324663.RALyW9YTcrRkeIogNcOmTEeSm1dN1bSNS1PHFnX9tLwJc
> .
@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#
> .
dgn-np:NP324663.RALyW9YTcrRkeIogNcOmTEeSm1dN1bSNS1PHFnX9tLwJc130_head
{
this:
np:hasAssertion
dgn-np:NP324663.RALyW9YTcrRkeIogNcOmTEeSm1dN1bSNS1PHFnX9tLwJc130_assertion
;
np:hasProvenance
dgn-np:NP324663.RALyW9YTcrRkeIogNcOmTEeSm1dN1bSNS1PHFnX9tLwJc130_provenance
;
np:hasPublicationInfo
dgn-np:NP324663.RALyW9YTcrRkeIogNcOmTEeSm1dN1bSNS1PHFnX9tLwJc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP324663.RALyW9YTcrRkeIogNcOmTEeSm1dN1bSNS1PHFnX9tLwJc130_assertion
a
np:Assertion
.
dgn-np:NP324663.RALyW9YTcrRkeIogNcOmTEeSm1dN1bSNS1PHFnX9tLwJc130_provenance
a
np:Provenance
.
dgn-np:NP324663.RALyW9YTcrRkeIogNcOmTEeSm1dN1bSNS1PHFnX9tLwJc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP324663.RALyW9YTcrRkeIogNcOmTEeSm1dN1bSNS1PHFnX9tLwJc130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0031511
a
ncit:C7057
.
dgn-gda:DGN443d7c625cf1f0a550cbf707491942b0
sio:SIO_000628
miriam-gene:7157
,
lld:C0031511
;
a
sio:SIO_001121
.
}
dgn-np:NP324663.RALyW9YTcrRkeIogNcOmTEeSm1dN1bSNS1PHFnX9tLwJc130_provenance
{
dgn-np:NP324663.RALyW9YTcrRkeIogNcOmTEeSm1dN1bSNS1PHFnX9tLwJc130_assertion
dcterms:description
"[The role of the TP53 gene in the development of inherited and sporadic pheochromocytomas and medullary thyroid carcinomas (MTC) has not been clarified because of conflicting reports and limitations in the assays used to detect mutations.]. 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:9290950
;
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:NP324663.RALyW9YTcrRkeIogNcOmTEeSm1dN1bSNS1PHFnX9tLwJc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:10+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
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}