@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP707775.RASb5LnAprBuW-1k6-kDhlNsPhg88ULerrkc_n88Mn-Lw
> .
@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:NP707775.RASb5LnAprBuW-1k6-kDhlNsPhg88ULerrkc_n88Mn-Lw130_head
{
this:
np:hasAssertion
dgn-np:NP707775.RASb5LnAprBuW-1k6-kDhlNsPhg88ULerrkc_n88Mn-Lw130_assertion
;
np:hasProvenance
dgn-np:NP707775.RASb5LnAprBuW-1k6-kDhlNsPhg88ULerrkc_n88Mn-Lw130_provenance
;
np:hasPublicationInfo
dgn-np:NP707775.RASb5LnAprBuW-1k6-kDhlNsPhg88ULerrkc_n88Mn-Lw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP707775.RASb5LnAprBuW-1k6-kDhlNsPhg88ULerrkc_n88Mn-Lw130_assertion
a
np:Assertion
.
dgn-np:NP707775.RASb5LnAprBuW-1k6-kDhlNsPhg88ULerrkc_n88Mn-Lw130_provenance
a
np:Provenance
.
dgn-np:NP707775.RASb5LnAprBuW-1k6-kDhlNsPhg88ULerrkc_n88Mn-Lw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP707775.RASb5LnAprBuW-1k6-kDhlNsPhg88ULerrkc_n88Mn-Lw130_assertion
{
miriam-gene:100128922
a
ncit:C16612
.
lld:C0018801
a
ncit:C7057
.
dgn-gda:DGN9603c61b7202ca376addf058d7767594
sio:SIO_000628
miriam-gene:100128922
,
lld:C0018801
;
a
sio:SIO_001121
.
}
dgn-np:NP707775.RASb5LnAprBuW-1k6-kDhlNsPhg88ULerrkc_n88Mn-Lw130_provenance
{
dgn-np:NP707775.RASb5LnAprBuW-1k6-kDhlNsPhg88ULerrkc_n88Mn-Lw130_assertion
dcterms:description
"[Although much is known about expression patterns and remodeling of cardiac connexin(Cx)43, little is known about the less abundant Cx45, which is required for embryonic development and viability, is downregulated in adult hearts, and is pathophysiologically upregulated in human end-stage heart failure.]. 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:22127232
;
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:NP707775.RASb5LnAprBuW-1k6-kDhlNsPhg88ULerrkc_n88Mn-Lw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:10+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" .
}