@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP843671.RARSlxKzPTnCheT1y_ZdJitMQE2RG5hgDKBqo3OMFi3gw
> .
@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:NP843671.RARSlxKzPTnCheT1y_ZdJitMQE2RG5hgDKBqo3OMFi3gw130_head
{
this:
np:hasAssertion
dgn-np:NP843671.RARSlxKzPTnCheT1y_ZdJitMQE2RG5hgDKBqo3OMFi3gw130_assertion
;
np:hasProvenance
dgn-np:NP843671.RARSlxKzPTnCheT1y_ZdJitMQE2RG5hgDKBqo3OMFi3gw130_provenance
;
np:hasPublicationInfo
dgn-np:NP843671.RARSlxKzPTnCheT1y_ZdJitMQE2RG5hgDKBqo3OMFi3gw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP843671.RARSlxKzPTnCheT1y_ZdJitMQE2RG5hgDKBqo3OMFi3gw130_assertion
a
np:Assertion
.
dgn-np:NP843671.RARSlxKzPTnCheT1y_ZdJitMQE2RG5hgDKBqo3OMFi3gw130_provenance
a
np:Provenance
.
dgn-np:NP843671.RARSlxKzPTnCheT1y_ZdJitMQE2RG5hgDKBqo3OMFi3gw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP843671.RARSlxKzPTnCheT1y_ZdJitMQE2RG5hgDKBqo3OMFi3gw130_assertion
{
miriam-gene:4233
a
ncit:C16612
.
lld:C0595905
a
ncit:C7057
.
dgn-gda:DGN577f7ca9680b1edadf8a0bb461cb1db8
sio:SIO_000628
miriam-gene:4233
,
lld:C0595905
;
a
sio:SIO_001121
.
}
dgn-np:NP843671.RARSlxKzPTnCheT1y_ZdJitMQE2RG5hgDKBqo3OMFi3gw130_provenance
{
dgn-np:NP843671.RARSlxKzPTnCheT1y_ZdJitMQE2RG5hgDKBqo3OMFi3gw130_assertion
dcterms:description
"[A functional variant in the promoter of the gene encoding the MET receptor tyrosine kinase is associated with autism spectrum disorder, and MET protein expression is decreased in the temporal cortex of subjects with autism spectrum disorder.]. 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:19255034
;
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:NP843671.RARSlxKzPTnCheT1y_ZdJitMQE2RG5hgDKBqo3OMFi3gw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:35+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" .
}