@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP174603.RAMV2wZAvqvgpkG_9cPhtad66q3Ci5OTc6uBQm0MFFs50
> .
@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:NP174603.RAMV2wZAvqvgpkG_9cPhtad66q3Ci5OTc6uBQm0MFFs50130_head
{
this:
np:hasAssertion
dgn-np:NP174603.RAMV2wZAvqvgpkG_9cPhtad66q3Ci5OTc6uBQm0MFFs50130_assertion
;
np:hasProvenance
dgn-np:NP174603.RAMV2wZAvqvgpkG_9cPhtad66q3Ci5OTc6uBQm0MFFs50130_provenance
;
np:hasPublicationInfo
dgn-np:NP174603.RAMV2wZAvqvgpkG_9cPhtad66q3Ci5OTc6uBQm0MFFs50130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP174603.RAMV2wZAvqvgpkG_9cPhtad66q3Ci5OTc6uBQm0MFFs50130_assertion
a
np:Assertion
.
dgn-np:NP174603.RAMV2wZAvqvgpkG_9cPhtad66q3Ci5OTc6uBQm0MFFs50130_provenance
a
np:Provenance
.
dgn-np:NP174603.RAMV2wZAvqvgpkG_9cPhtad66q3Ci5OTc6uBQm0MFFs50130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP174603.RAMV2wZAvqvgpkG_9cPhtad66q3Ci5OTc6uBQm0MFFs50130_assertion
{
miriam-gene:57045
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGNb03499d06e7634a761e15c607360ff87
sio:SIO_000628
miriam-gene:57045
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP174603.RAMV2wZAvqvgpkG_9cPhtad66q3Ci5OTc6uBQm0MFFs50130_provenance
{
dgn-np:NP174603.RAMV2wZAvqvgpkG_9cPhtad66q3Ci5OTc6uBQm0MFFs50130_assertion
dcterms:description
"[The data suggest that LOH from 8p is frequent in human breast cancers and that loss of the putative 8p TSG may be an important event in early stage 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:7669738
;
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:NP174603.RAMV2wZAvqvgpkG_9cPhtad66q3Ci5OTc6uBQm0MFFs50130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:34+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" .
}