@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc
> .
@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:NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_head
{
this:
np:hasAssertion
dgn-np:NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_assertion
;
np:hasProvenance
dgn-np:NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_provenance
;
np:hasPublicationInfo
dgn-np:NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_assertion
a
np:Assertion
.
dgn-np:NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_provenance
a
np:Provenance
.
dgn-np:NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_assertion
{
miriam-gene:1063
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN38bcb30453e0a8fbe57b7adf64946cfc
sio:SIO_000628
miriam-gene:1063
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_provenance
{
dgn-np:NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_assertion
dcterms:description
"[As there is increasing evidence that CENPF is associated with poor prognosis in patients with primary BC, further independent studies are needed to clarify the importance of genetic variation in the CENPF gene in the clinic.]. 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:19008095
;
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:NP470078.RA7lDN4rcyGlFkZBe8UENg2dm5qvijm8tOiJpnAcwELsc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:42+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" .
}