@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP426359.RAgmwrY2a9EL6ZEKUl0bFPiSr8WEBLZhXJsPAX5WT7__c
> .
@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:NP426359.RAgmwrY2a9EL6ZEKUl0bFPiSr8WEBLZhXJsPAX5WT7__c130_head
{
this:
np:hasAssertion
dgn-np:NP426359.RAgmwrY2a9EL6ZEKUl0bFPiSr8WEBLZhXJsPAX5WT7__c130_assertion
;
np:hasProvenance
dgn-np:NP426359.RAgmwrY2a9EL6ZEKUl0bFPiSr8WEBLZhXJsPAX5WT7__c130_provenance
;
np:hasPublicationInfo
dgn-np:NP426359.RAgmwrY2a9EL6ZEKUl0bFPiSr8WEBLZhXJsPAX5WT7__c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP426359.RAgmwrY2a9EL6ZEKUl0bFPiSr8WEBLZhXJsPAX5WT7__c130_assertion
a
np:Assertion
.
dgn-np:NP426359.RAgmwrY2a9EL6ZEKUl0bFPiSr8WEBLZhXJsPAX5WT7__c130_provenance
a
np:Provenance
.
dgn-np:NP426359.RAgmwrY2a9EL6ZEKUl0bFPiSr8WEBLZhXJsPAX5WT7__c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP426359.RAgmwrY2a9EL6ZEKUl0bFPiSr8WEBLZhXJsPAX5WT7__c130_assertion
{
miriam-gene:22854
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN0ec0f87d4d1ec2c60c4f451ef6a8ccab
sio:SIO_000628
miriam-gene:22854
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP426359.RAgmwrY2a9EL6ZEKUl0bFPiSr8WEBLZhXJsPAX5WT7__c130_provenance
{
dgn-np:NP426359.RAgmwrY2a9EL6ZEKUl0bFPiSr8WEBLZhXJsPAX5WT7__c130_assertion
dcterms:description
"[These genes presumably derived from gene duplications, and they are highly similar to Deleted in Colorectal Cancer (DCC), which functions as an axon guidance molecule during development of the nervous system.]. 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:11318607
;
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:NP426359.RAgmwrY2a9EL6ZEKUl0bFPiSr8WEBLZhXJsPAX5WT7__c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:13+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" .
}