@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP828094.RAYqEk7_AnMYti3CiRXL68RUjDknvHliDITdg-uvjH-hg
> .
@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:NP828094.RAYqEk7_AnMYti3CiRXL68RUjDknvHliDITdg-uvjH-hg130_head
{
this:
np:hasAssertion
dgn-np:NP828094.RAYqEk7_AnMYti3CiRXL68RUjDknvHliDITdg-uvjH-hg130_assertion
;
np:hasProvenance
dgn-np:NP828094.RAYqEk7_AnMYti3CiRXL68RUjDknvHliDITdg-uvjH-hg130_provenance
;
np:hasPublicationInfo
dgn-np:NP828094.RAYqEk7_AnMYti3CiRXL68RUjDknvHliDITdg-uvjH-hg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP828094.RAYqEk7_AnMYti3CiRXL68RUjDknvHliDITdg-uvjH-hg130_assertion
a
np:Assertion
.
dgn-np:NP828094.RAYqEk7_AnMYti3CiRXL68RUjDknvHliDITdg-uvjH-hg130_provenance
a
np:Provenance
.
dgn-np:NP828094.RAYqEk7_AnMYti3CiRXL68RUjDknvHliDITdg-uvjH-hg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP828094.RAYqEk7_AnMYti3CiRXL68RUjDknvHliDITdg-uvjH-hg130_assertion
{
miriam-gene:6722
a
ncit:C16612
.
lld:C0018802
a
ncit:C7057
.
dgn-gda:DGN59e795a1b1724431a2617b8709459fae
sio:SIO_000628
miriam-gene:6722
,
lld:C0018802
;
a
sio:SIO_001121
.
}
dgn-np:NP828094.RAYqEk7_AnMYti3CiRXL68RUjDknvHliDITdg-uvjH-hg130_provenance
{
dgn-np:NP828094.RAYqEk7_AnMYti3CiRXL68RUjDknvHliDITdg-uvjH-hg130_assertion
dcterms:description
"[We suggest that the rapid progression to heart failure in SRF mutant mice results primarily from decreased expression of proteins involved in force generation and transmission, low levels of polymerized actin, and changes in cytoarchitecture, without hypertrophic compensation.]. 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:16260633
;
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:NP828094.RAYqEk7_AnMYti3CiRXL68RUjDknvHliDITdg-uvjH-hg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:27+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" .
}