@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP837737.RA7TRlyOEiGcvIQ3tpAe3W9TkZdNbHVTeDf2la9g0IVI4
> .
@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:NP837737.RA7TRlyOEiGcvIQ3tpAe3W9TkZdNbHVTeDf2la9g0IVI4130_head
{
this:
np:hasAssertion
dgn-np:NP837737.RA7TRlyOEiGcvIQ3tpAe3W9TkZdNbHVTeDf2la9g0IVI4130_assertion
;
np:hasProvenance
dgn-np:NP837737.RA7TRlyOEiGcvIQ3tpAe3W9TkZdNbHVTeDf2la9g0IVI4130_provenance
;
np:hasPublicationInfo
dgn-np:NP837737.RA7TRlyOEiGcvIQ3tpAe3W9TkZdNbHVTeDf2la9g0IVI4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP837737.RA7TRlyOEiGcvIQ3tpAe3W9TkZdNbHVTeDf2la9g0IVI4130_assertion
a
np:Assertion
.
dgn-np:NP837737.RA7TRlyOEiGcvIQ3tpAe3W9TkZdNbHVTeDf2la9g0IVI4130_provenance
a
np:Provenance
.
dgn-np:NP837737.RA7TRlyOEiGcvIQ3tpAe3W9TkZdNbHVTeDf2la9g0IVI4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP837737.RA7TRlyOEiGcvIQ3tpAe3W9TkZdNbHVTeDf2la9g0IVI4130_assertion
{
miriam-gene:10243
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN2d8d9efe42881109e6f3bcf3533eec25
sio:SIO_000628
miriam-gene:10243
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP837737.RA7TRlyOEiGcvIQ3tpAe3W9TkZdNbHVTeDf2la9g0IVI4130_provenance
{
dgn-np:NP837737.RA7TRlyOEiGcvIQ3tpAe3W9TkZdNbHVTeDf2la9g0IVI4130_assertion
dcterms:description
"[The hypermutability and the specific p53 mutations involving the biologically functional domain (e.g., zinc binding domain or DNA contact region) have an insignificant influence on invasive progression in the breast cancer.]. 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:11715068
;
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:NP837737.RA7TRlyOEiGcvIQ3tpAe3W9TkZdNbHVTeDf2la9g0IVI4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:32+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" .
}