@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_head
{
this:
np:hasAssertion
dgn-np:NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_assertion
;
np:hasProvenance
dgn-np:NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_provenance
;
np:hasPublicationInfo
dgn-np:NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_assertion
a
np:Assertion
.
dgn-np:NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_provenance
a
np:Provenance
.
dgn-np:NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_assertion
{
miriam-gene:10370
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGN6919df67ebd428d0a43ce194f019dfd6
sio:SIO_000628
miriam-gene:10370
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_provenance
{
dgn-np:NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_assertion
dcterms:description
"[These results indicate that the SRJ domain is dispensable for these functions of CITED2 in mice and that mutations clustering in the SRJ region are unlikely to be the sole cause of the malformations observed in patients with sporadic CHD.]. 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:23082118
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP841331.RAlxFxho02OKuMdRLaGZaG9e1g7HZqAYvtmcNVGDpKezY130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:11+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}