@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg
> .
@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:NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_head
{
this:
np:hasAssertion
dgn-np:NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_assertion
;
np:hasProvenance
dgn-np:NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_provenance
;
np:hasPublicationInfo
dgn-np:NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_assertion
a
np:Assertion
.
dgn-np:NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_provenance
a
np:Provenance
.
dgn-np:NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_assertion
{
miriam-gene:78987
a
ncit:C16612
.
lld:C1389016
a
ncit:C7057
.
dgn-gda:DGN731e0ca14e3bbbd6f424986937ea6da7
sio:SIO_000628
miriam-gene:78987
,
lld:C1389016
;
a
sio:SIO_001121
.
}
dgn-np:NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_provenance
{
dgn-np:NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_assertion
dcterms:description
"[CRELD1 is the first human gene to be implicated in the pathogenesis of isolated AVSD and AVSD in the context of heterotaxy, which provides an important step in unraveling the pathogenesis of AVSD.]. 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:12632326
;
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:NP227845.RAUbNlgZHHLy1BP9HIFJcVnMkL1gSeBosROb7nSpJhiFg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:06+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" .
}