@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP540683.RAvJmWb0n42Oc96NmeiAhzOsXIzNUBhHSVRT1pfEq2IXo
> .
@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:NP540683.RAvJmWb0n42Oc96NmeiAhzOsXIzNUBhHSVRT1pfEq2IXo130_head
{
this:
np:hasAssertion
dgn-np:NP540683.RAvJmWb0n42Oc96NmeiAhzOsXIzNUBhHSVRT1pfEq2IXo130_assertion
;
np:hasProvenance
dgn-np:NP540683.RAvJmWb0n42Oc96NmeiAhzOsXIzNUBhHSVRT1pfEq2IXo130_provenance
;
np:hasPublicationInfo
dgn-np:NP540683.RAvJmWb0n42Oc96NmeiAhzOsXIzNUBhHSVRT1pfEq2IXo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP540683.RAvJmWb0n42Oc96NmeiAhzOsXIzNUBhHSVRT1pfEq2IXo130_assertion
a
np:Assertion
.
dgn-np:NP540683.RAvJmWb0n42Oc96NmeiAhzOsXIzNUBhHSVRT1pfEq2IXo130_provenance
a
np:Provenance
.
dgn-np:NP540683.RAvJmWb0n42Oc96NmeiAhzOsXIzNUBhHSVRT1pfEq2IXo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP540683.RAvJmWb0n42Oc96NmeiAhzOsXIzNUBhHSVRT1pfEq2IXo130_assertion
{
miriam-gene:145957
a
ncit:C16612
.
lld:C0009319
a
ncit:C7057
.
dgn-gda:DGN1f636dee7bad8bce03ba93fa15259faa
sio:SIO_000628
miriam-gene:145957
,
lld:C0009319
;
a
sio:SIO_001121
.
}
dgn-np:NP540683.RAvJmWb0n42Oc96NmeiAhzOsXIzNUBhHSVRT1pfEq2IXo130_provenance
{
dgn-np:NP540683.RAvJmWb0n42Oc96NmeiAhzOsXIzNUBhHSVRT1pfEq2IXo130_assertion
dcterms:description
"[With regard to the potential clinical importance of this pathway, NRG4 expression was decreased in human inflammatory bowel disease samples and mouse models of colitis, suggesting that activation of ErbB4 is altered in disease.]. 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:23033483
;
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:NP540683.RAvJmWb0n42Oc96NmeiAhzOsXIzNUBhHSVRT1pfEq2IXo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:26+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" .
}