@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP810603.RALXBCF6PqaGTKfwlKKIzr-i_cP_XSTtqfB2rXKFmuJcY
> .
@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:NP810603.RALXBCF6PqaGTKfwlKKIzr-i_cP_XSTtqfB2rXKFmuJcY130_head
{
this:
np:hasAssertion
dgn-np:NP810603.RALXBCF6PqaGTKfwlKKIzr-i_cP_XSTtqfB2rXKFmuJcY130_assertion
;
np:hasProvenance
dgn-np:NP810603.RALXBCF6PqaGTKfwlKKIzr-i_cP_XSTtqfB2rXKFmuJcY130_provenance
;
np:hasPublicationInfo
dgn-np:NP810603.RALXBCF6PqaGTKfwlKKIzr-i_cP_XSTtqfB2rXKFmuJcY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP810603.RALXBCF6PqaGTKfwlKKIzr-i_cP_XSTtqfB2rXKFmuJcY130_assertion
a
np:Assertion
.
dgn-np:NP810603.RALXBCF6PqaGTKfwlKKIzr-i_cP_XSTtqfB2rXKFmuJcY130_provenance
a
np:Provenance
.
dgn-np:NP810603.RALXBCF6PqaGTKfwlKKIzr-i_cP_XSTtqfB2rXKFmuJcY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP810603.RALXBCF6PqaGTKfwlKKIzr-i_cP_XSTtqfB2rXKFmuJcY130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C1449563
a
ncit:C7057
.
dgn-gda:DGN33d6814c981f5c363be14306304cb9c0
sio:SIO_000628
miriam-gene:3342
,
lld:C1449563
;
a
sio:SIO_001121
.
}
dgn-np:NP810603.RALXBCF6PqaGTKfwlKKIzr-i_cP_XSTtqfB2rXKFmuJcY130_provenance
{
dgn-np:NP810603.RALXBCF6PqaGTKfwlKKIzr-i_cP_XSTtqfB2rXKFmuJcY130_assertion
dcterms:description
"[In 5 patients, comparative genomic hybridization (CGH) after laser microdissection revealed 20q13 amplification in four of five cases of IH, in all of three cases of IH with atypia, all five of DCIS, and all five of IDC.]. 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:10592049
;
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:NP810603.RALXBCF6PqaGTKfwlKKIzr-i_cP_XSTtqfB2rXKFmuJcY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:17+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" .
}