@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8
> .
@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:NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8130_head
{
this:
np:hasAssertion
dgn-np:NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8130_assertion
;
np:hasProvenance
dgn-np:NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8130_provenance
;
np:hasPublicationInfo
dgn-np:NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8130_assertion
a
np:Assertion
.
dgn-np:NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8130_provenance
a
np:Provenance
.
dgn-np:NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8130_assertion
{
miriam-gene:3356
a
ncit:C16612
.
lld:C0003125
a
ncit:C7057
.
dgn-gda:DGN8a7324ebf90b6dd2e4d47e140e9cad04
sio:SIO_000628
miriam-gene:3356
,
lld:C0003125
;
a
sio:SIO_001121
.
}
dgn-np:NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8130_provenance
{
dgn-np:NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8130_assertion
dcterms:description
"[Although, at present, no convincing evidence for associations of candidate genes with EDs has been provided, the 5-HT(2A) receptor gene and the BDNF gene seem to be promising candidates for genetic influences on AN, since polymorphic variants of these genes have been found quite consistently, although not specifically, linked to AN restricting subtype in large sample studies.]. 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:18855537
;
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:NP808536.RADmaJayt50co7kDEkGk0oxnxYoT7pH8GzNXds1ykPcf8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:16+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" .
}