@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP717437.RAJp3P3_1A44ufPv2bAh2vkzaZsRK8o_WQGgQT7XztEbQ
> .
@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:NP717437.RAJp3P3_1A44ufPv2bAh2vkzaZsRK8o_WQGgQT7XztEbQ130_head
{
this:
np:hasAssertion
dgn-np:NP717437.RAJp3P3_1A44ufPv2bAh2vkzaZsRK8o_WQGgQT7XztEbQ130_assertion
;
np:hasProvenance
dgn-np:NP717437.RAJp3P3_1A44ufPv2bAh2vkzaZsRK8o_WQGgQT7XztEbQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP717437.RAJp3P3_1A44ufPv2bAh2vkzaZsRK8o_WQGgQT7XztEbQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP717437.RAJp3P3_1A44ufPv2bAh2vkzaZsRK8o_WQGgQT7XztEbQ130_assertion
a
np:Assertion
.
dgn-np:NP717437.RAJp3P3_1A44ufPv2bAh2vkzaZsRK8o_WQGgQT7XztEbQ130_provenance
a
np:Provenance
.
dgn-np:NP717437.RAJp3P3_1A44ufPv2bAh2vkzaZsRK8o_WQGgQT7XztEbQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP717437.RAJp3P3_1A44ufPv2bAh2vkzaZsRK8o_WQGgQT7XztEbQ130_assertion
{
miriam-gene:129684
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGN2cf27fe9d026243d3a162613777b7ba1
sio:SIO_000628
miriam-gene:129684
,
lld:C0004352
;
a
sio:SIO_001121
.
}
dgn-np:NP717437.RAJp3P3_1A44ufPv2bAh2vkzaZsRK8o_WQGgQT7XztEbQ130_provenance
{
dgn-np:NP717437.RAJp3P3_1A44ufPv2bAh2vkzaZsRK8o_WQGgQT7XztEbQ130_assertion
dcterms:description
"[We speculate that loss of CNTNAP5 might contribute to the developmental language delay of this patient, similar to CNTNAP2, another member of the same protein family, whose alterations have been recently associated with delay in the age at first word in autistic patients.]. 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:19236961
;
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:NP717437.RAJp3P3_1A44ufPv2bAh2vkzaZsRK8o_WQGgQT7XztEbQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:15+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" .
}