@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP159541.RAKJgf6CA-vWXeQ7cfIyxFba5fe5rMnGS7Z0VXk9FTDK8
> .
@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:NP159541.RAKJgf6CA-vWXeQ7cfIyxFba5fe5rMnGS7Z0VXk9FTDK8130_head
{
this:
np:hasAssertion
dgn-np:NP159541.RAKJgf6CA-vWXeQ7cfIyxFba5fe5rMnGS7Z0VXk9FTDK8130_assertion
;
np:hasProvenance
dgn-np:NP159541.RAKJgf6CA-vWXeQ7cfIyxFba5fe5rMnGS7Z0VXk9FTDK8130_provenance
;
np:hasPublicationInfo
dgn-np:NP159541.RAKJgf6CA-vWXeQ7cfIyxFba5fe5rMnGS7Z0VXk9FTDK8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP159541.RAKJgf6CA-vWXeQ7cfIyxFba5fe5rMnGS7Z0VXk9FTDK8130_assertion
a
np:Assertion
.
dgn-np:NP159541.RAKJgf6CA-vWXeQ7cfIyxFba5fe5rMnGS7Z0VXk9FTDK8130_provenance
a
np:Provenance
.
dgn-np:NP159541.RAKJgf6CA-vWXeQ7cfIyxFba5fe5rMnGS7Z0VXk9FTDK8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP159541.RAKJgf6CA-vWXeQ7cfIyxFba5fe5rMnGS7Z0VXk9FTDK8130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN4176701b765974f9397feca7fbb2a345
sio:SIO_000628
miriam-gene:7157
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP159541.RAKJgf6CA-vWXeQ7cfIyxFba5fe5rMnGS7Z0VXk9FTDK8130_provenance
{
dgn-np:NP159541.RAKJgf6CA-vWXeQ7cfIyxFba5fe5rMnGS7Z0VXk9FTDK8130_assertion
dcterms:description
"[These findings indicate that not just p53 mutation per se but the full spectrum (i.e., different types, locations, and numbers) of p53 mutation needs to be examined when it is used as a prognostic marker of survival in breast cancer patients.]. 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:14997055
;
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:NP159541.RAKJgf6CA-vWXeQ7cfIyxFba5fe5rMnGS7Z0VXk9FTDK8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:26+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" .
}