@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY
> .
@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:NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY130_head
{
this:
np:hasAssertion
dgn-np:NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY130_assertion
;
np:hasProvenance
dgn-np:NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY130_provenance
;
np:hasPublicationInfo
dgn-np:NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY130_assertion
a
np:Assertion
.
dgn-np:NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY130_provenance
a
np:Provenance
.
dgn-np:NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0206644
a
ncit:C7057
.
dgn-gda:DGN523cc8ad2daa6f38bdf441c29c74acb6
sio:SIO_000628
miriam-gene:7157
,
lld:C0206644
;
a
sio:SIO_001121
.
}
dgn-np:NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY130_provenance
{
dgn-np:NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY130_assertion
dcterms:description
"[However, a similar staining pattern in apparently normal tissue was also observed in 13/48 sections from other individuals with various skin conditions (melanocytic naevi, psoriasis and normal skin adjacent to malignant melanoma and fibrous histiocytomas), suggesting that this pattern of p53 staining may not be unique to individuals with constitutional p53 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:8479749
;
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:NP900590.RAgWCOq0xHNIwanxnZWOAkoPC3VKGJBk3hGIDhTg9l0mY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:13+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" .
}