@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP755225.RAwzoQ0pyaLPNAzrOSZZkJwa-ANCHG25IZ39WkdyxqPP4
> .
@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:NP755225.RAwzoQ0pyaLPNAzrOSZZkJwa-ANCHG25IZ39WkdyxqPP4130_head
{
this:
np:hasAssertion
dgn-np:NP755225.RAwzoQ0pyaLPNAzrOSZZkJwa-ANCHG25IZ39WkdyxqPP4130_assertion
;
np:hasProvenance
dgn-np:NP755225.RAwzoQ0pyaLPNAzrOSZZkJwa-ANCHG25IZ39WkdyxqPP4130_provenance
;
np:hasPublicationInfo
dgn-np:NP755225.RAwzoQ0pyaLPNAzrOSZZkJwa-ANCHG25IZ39WkdyxqPP4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP755225.RAwzoQ0pyaLPNAzrOSZZkJwa-ANCHG25IZ39WkdyxqPP4130_assertion
a
np:Assertion
.
dgn-np:NP755225.RAwzoQ0pyaLPNAzrOSZZkJwa-ANCHG25IZ39WkdyxqPP4130_provenance
a
np:Provenance
.
dgn-np:NP755225.RAwzoQ0pyaLPNAzrOSZZkJwa-ANCHG25IZ39WkdyxqPP4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP755225.RAwzoQ0pyaLPNAzrOSZZkJwa-ANCHG25IZ39WkdyxqPP4130_assertion
{
miriam-gene:54858
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGN4a7234482ab3a01674e67a957c13a389
sio:SIO_000628
miriam-gene:54858
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP755225.RAwzoQ0pyaLPNAzrOSZZkJwa-ANCHG25IZ39WkdyxqPP4130_provenance
{
dgn-np:NP755225.RAwzoQ0pyaLPNAzrOSZZkJwa-ANCHG25IZ39WkdyxqPP4130_assertion
dcterms:description
"[The mutant genes that have been causative in disturbance of PCP in mouse models have been examined in human malformations but none of them have so far been implicated in human craniorachischisis.]. 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:19129707
;
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:NP755225.RAwzoQ0pyaLPNAzrOSZZkJwa-ANCHG25IZ39WkdyxqPP4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:37+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" .
}