@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP441657.RA1Qabv86sUfSZWRi8_zigeokAXdiZIj5gkm8HH1SeNEE
> .
@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:NP441657.RA1Qabv86sUfSZWRi8_zigeokAXdiZIj5gkm8HH1SeNEE130_head
{
this:
np:hasAssertion
dgn-np:NP441657.RA1Qabv86sUfSZWRi8_zigeokAXdiZIj5gkm8HH1SeNEE130_assertion
;
np:hasProvenance
dgn-np:NP441657.RA1Qabv86sUfSZWRi8_zigeokAXdiZIj5gkm8HH1SeNEE130_provenance
;
np:hasPublicationInfo
dgn-np:NP441657.RA1Qabv86sUfSZWRi8_zigeokAXdiZIj5gkm8HH1SeNEE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP441657.RA1Qabv86sUfSZWRi8_zigeokAXdiZIj5gkm8HH1SeNEE130_assertion
a
np:Assertion
.
dgn-np:NP441657.RA1Qabv86sUfSZWRi8_zigeokAXdiZIj5gkm8HH1SeNEE130_provenance
a
np:Provenance
.
dgn-np:NP441657.RA1Qabv86sUfSZWRi8_zigeokAXdiZIj5gkm8HH1SeNEE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP441657.RA1Qabv86sUfSZWRi8_zigeokAXdiZIj5gkm8HH1SeNEE130_assertion
{
miriam-gene:55034
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGNb7ab1866407493855c32b10e03c5ef8d
sio:SIO_000628
miriam-gene:55034
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP441657.RA1Qabv86sUfSZWRi8_zigeokAXdiZIj5gkm8HH1SeNEE130_provenance
{
dgn-np:NP441657.RA1Qabv86sUfSZWRi8_zigeokAXdiZIj5gkm8HH1SeNEE130_assertion
dcterms:description
"[After controlling for multiple comparisons and confounding effects of stage, five chromosomal aberrations were significantly associated with outcome, including amplification at 11q13, gain of 12q24, and losses at 5q11, 6q14, and 21q11 (MCS adjusted P =.0009 to P =.01).]. 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:15459219
;
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:NP441657.RA1Qabv86sUfSZWRi8_zigeokAXdiZIj5gkm8HH1SeNEE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:21+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" .
}