@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP402152.RA3nX1fw88i78QeIqq_C5H7GuShNthISLMjyiLYR4jwUU
> .
@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:NP402152.RA3nX1fw88i78QeIqq_C5H7GuShNthISLMjyiLYR4jwUU130_head
{
this:
np:hasAssertion
dgn-np:NP402152.RA3nX1fw88i78QeIqq_C5H7GuShNthISLMjyiLYR4jwUU130_assertion
;
np:hasProvenance
dgn-np:NP402152.RA3nX1fw88i78QeIqq_C5H7GuShNthISLMjyiLYR4jwUU130_provenance
;
np:hasPublicationInfo
dgn-np:NP402152.RA3nX1fw88i78QeIqq_C5H7GuShNthISLMjyiLYR4jwUU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP402152.RA3nX1fw88i78QeIqq_C5H7GuShNthISLMjyiLYR4jwUU130_assertion
a
np:Assertion
.
dgn-np:NP402152.RA3nX1fw88i78QeIqq_C5H7GuShNthISLMjyiLYR4jwUU130_provenance
a
np:Provenance
.
dgn-np:NP402152.RA3nX1fw88i78QeIqq_C5H7GuShNthISLMjyiLYR4jwUU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP402152.RA3nX1fw88i78QeIqq_C5H7GuShNthISLMjyiLYR4jwUU130_assertion
{
miriam-gene:10383
a
ncit:C16612
.
lld:C0004936
a
ncit:C7057
.
dgn-gda:DGN2d8a7b21234923e004f6f8403504cd4e
sio:SIO_000628
miriam-gene:10383
,
lld:C0004936
;
a
sio:SIO_001121
.
}
dgn-np:NP402152.RA3nX1fw88i78QeIqq_C5H7GuShNthISLMjyiLYR4jwUU130_provenance
{
dgn-np:NP402152.RA3nX1fw88i78QeIqq_C5H7GuShNthISLMjyiLYR4jwUU130_assertion
dcterms:description
"[This is a biologically plausible mechanism whereby beta 2 adrenergic agonists can induce functional and behavioral teratogenesis, which explains their association with increases in autism spectrum disorders, psychiatric disorders, poor cognitive, motor function and school performance, and changes in blood pressure in the offspring.]. 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:19961985
;
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:NP402152.RA3nX1fw88i78QeIqq_C5H7GuShNthISLMjyiLYR4jwUU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:59+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" .
}