@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP784585.RAYDNsJlHj38eBLqx1tfwNzgaSp4m_K49Yb70v4Xq7caI
> .
@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:NP784585.RAYDNsJlHj38eBLqx1tfwNzgaSp4m_K49Yb70v4Xq7caI130_head
{
this:
np:hasAssertion
dgn-np:NP784585.RAYDNsJlHj38eBLqx1tfwNzgaSp4m_K49Yb70v4Xq7caI130_assertion
;
np:hasProvenance
dgn-np:NP784585.RAYDNsJlHj38eBLqx1tfwNzgaSp4m_K49Yb70v4Xq7caI130_provenance
;
np:hasPublicationInfo
dgn-np:NP784585.RAYDNsJlHj38eBLqx1tfwNzgaSp4m_K49Yb70v4Xq7caI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP784585.RAYDNsJlHj38eBLqx1tfwNzgaSp4m_K49Yb70v4Xq7caI130_assertion
a
np:Assertion
.
dgn-np:NP784585.RAYDNsJlHj38eBLqx1tfwNzgaSp4m_K49Yb70v4Xq7caI130_provenance
a
np:Provenance
.
dgn-np:NP784585.RAYDNsJlHj38eBLqx1tfwNzgaSp4m_K49Yb70v4Xq7caI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP784585.RAYDNsJlHj38eBLqx1tfwNzgaSp4m_K49Yb70v4Xq7caI130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0220603
a
ncit:C7057
.
dgn-gda:DGN90954d1809fcae70021ebca98450ba97
sio:SIO_000628
miriam-gene:7157
,
lld:C0220603
;
a
sio:SIO_001121
.
}
dgn-np:NP784585.RAYDNsJlHj38eBLqx1tfwNzgaSp4m_K49Yb70v4Xq7caI130_provenance
{
dgn-np:NP784585.RAYDNsJlHj38eBLqx1tfwNzgaSp4m_K49Yb70v4Xq7caI130_assertion
dcterms:description
"[Although mutation of the TP53 gene located on 17p is the most frequent genetic mutation in all adult tumor types, such mutations are rare in most childhood brain tumors investigated to date.]. 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:8889505
;
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:NP784585.RAYDNsJlHj38eBLqx1tfwNzgaSp4m_K49Yb70v4Xq7caI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:55+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" .
}