@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP573932.RAHK5kDSYupHPW3f2v5ykIyTgNcv_uzHZNs9qIZfMZRQI
> .
@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/v4.0.0/void/
> .
dgn-np:NP573932.RAHK5kDSYupHPW3f2v5ykIyTgNcv_uzHZNs9qIZfMZRQI130_head
{
this:
np:hasAssertion
dgn-np:NP573932.RAHK5kDSYupHPW3f2v5ykIyTgNcv_uzHZNs9qIZfMZRQI130_assertion
;
np:hasProvenance
dgn-np:NP573932.RAHK5kDSYupHPW3f2v5ykIyTgNcv_uzHZNs9qIZfMZRQI130_provenance
;
np:hasPublicationInfo
dgn-np:NP573932.RAHK5kDSYupHPW3f2v5ykIyTgNcv_uzHZNs9qIZfMZRQI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP573932.RAHK5kDSYupHPW3f2v5ykIyTgNcv_uzHZNs9qIZfMZRQI130_assertion
a
np:Assertion
.
dgn-np:NP573932.RAHK5kDSYupHPW3f2v5ykIyTgNcv_uzHZNs9qIZfMZRQI130_provenance
a
np:Provenance
.
dgn-np:NP573932.RAHK5kDSYupHPW3f2v5ykIyTgNcv_uzHZNs9qIZfMZRQI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP573932.RAHK5kDSYupHPW3f2v5ykIyTgNcv_uzHZNs9qIZfMZRQI130_assertion
{
miriam-gene:93986
a
ncit:C16612
.
lld:C0023009
a
ncit:C7057
.
dgn-gda:DGN6465db6578a507d5e1ede9a106464ad3
sio:SIO_000628
miriam-gene:93986
,
lld:C0023009
;
a
sio:SIO_001121
.
}
dgn-np:NP573932.RAHK5kDSYupHPW3f2v5ykIyTgNcv_uzHZNs9qIZfMZRQI130_provenance
{
dgn-np:NP573932.RAHK5kDSYupHPW3f2v5ykIyTgNcv_uzHZNs9qIZfMZRQI130_assertion
dcterms:description
"[In 2001, a point mutation in the forkhead box P2 (FOXP2) coding sequence was identified as the basis of an inherited speech and language disorder suffered by members of the family known as KE. This mini-symposium review focuses on recent findings and research-in-progress, primarily from five laboratories.]. 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:17035521
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP573932.RAHK5kDSYupHPW3f2v5ykIyTgNcv_uzHZNs9qIZfMZRQI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:05+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}