@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP869816.RAs6-ENLcd5RV-89T0vaVy2THXRyPz16yPCMZ7rxb8edw
> .
@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:NP869816.RAs6-ENLcd5RV-89T0vaVy2THXRyPz16yPCMZ7rxb8edw130_head
{
this:
np:hasAssertion
dgn-np:NP869816.RAs6-ENLcd5RV-89T0vaVy2THXRyPz16yPCMZ7rxb8edw130_assertion
;
np:hasProvenance
dgn-np:NP869816.RAs6-ENLcd5RV-89T0vaVy2THXRyPz16yPCMZ7rxb8edw130_provenance
;
np:hasPublicationInfo
dgn-np:NP869816.RAs6-ENLcd5RV-89T0vaVy2THXRyPz16yPCMZ7rxb8edw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP869816.RAs6-ENLcd5RV-89T0vaVy2THXRyPz16yPCMZ7rxb8edw130_assertion
a
np:Assertion
.
dgn-np:NP869816.RAs6-ENLcd5RV-89T0vaVy2THXRyPz16yPCMZ7rxb8edw130_provenance
a
np:Provenance
.
dgn-np:NP869816.RAs6-ENLcd5RV-89T0vaVy2THXRyPz16yPCMZ7rxb8edw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP869816.RAs6-ENLcd5RV-89T0vaVy2THXRyPz16yPCMZ7rxb8edw130_assertion
{
miriam-gene:28996
a
ncit:C16612
.
lld:C1800706
a
ncit:C7057
.
dgn-gda:DGNf1a37ed2777b6469998de945d320456d
sio:SIO_000628
miriam-gene:28996
,
lld:C1800706
;
a
sio:SIO_001121
.
}
dgn-np:NP869816.RAs6-ENLcd5RV-89T0vaVy2THXRyPz16yPCMZ7rxb8edw130_provenance
{
dgn-np:NP869816.RAs6-ENLcd5RV-89T0vaVy2THXRyPz16yPCMZ7rxb8edw130_assertion
dcterms:description
"[Aim of the present study was to analyze the loss of heterozygosity (LOH) at HIPK2 locus 7q32.34 in human lung fibroblasts and the HIPK2 expression in 15 IPF samples and in four primary fibroblast cell cultures isolated from IPF biopsies using semi-quantitative RT-PCR, Western blots and immunohistochemistry.]. 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:22689412
;
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:NP869816.RAs6-ENLcd5RV-89T0vaVy2THXRyPz16yPCMZ7rxb8edw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:52+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" .
}