@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP703496.RAIpZYuyktdX34dM9c0WE4jxNOS9eLsPC7lmx6Vgkra4o
> .
@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:NP703496.RAIpZYuyktdX34dM9c0WE4jxNOS9eLsPC7lmx6Vgkra4o130_head
{
this:
np:hasAssertion
dgn-np:NP703496.RAIpZYuyktdX34dM9c0WE4jxNOS9eLsPC7lmx6Vgkra4o130_assertion
;
np:hasProvenance
dgn-np:NP703496.RAIpZYuyktdX34dM9c0WE4jxNOS9eLsPC7lmx6Vgkra4o130_provenance
;
np:hasPublicationInfo
dgn-np:NP703496.RAIpZYuyktdX34dM9c0WE4jxNOS9eLsPC7lmx6Vgkra4o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP703496.RAIpZYuyktdX34dM9c0WE4jxNOS9eLsPC7lmx6Vgkra4o130_assertion
a
np:Assertion
.
dgn-np:NP703496.RAIpZYuyktdX34dM9c0WE4jxNOS9eLsPC7lmx6Vgkra4o130_provenance
a
np:Provenance
.
dgn-np:NP703496.RAIpZYuyktdX34dM9c0WE4jxNOS9eLsPC7lmx6Vgkra4o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP703496.RAIpZYuyktdX34dM9c0WE4jxNOS9eLsPC7lmx6Vgkra4o130_assertion
{
miriam-gene:3240
a
ncit:C16612
.
lld:C0525045
a
ncit:C7057
.
dgn-gda:DGN5ebeb54e5fdbaad1ccde36e94bda5e57
sio:SIO_000628
miriam-gene:3240
,
lld:C0525045
;
a
sio:SIO_001121
.
}
dgn-np:NP703496.RAIpZYuyktdX34dM9c0WE4jxNOS9eLsPC7lmx6Vgkra4o130_provenance
{
dgn-np:NP703496.RAIpZYuyktdX34dM9c0WE4jxNOS9eLsPC7lmx6Vgkra4o130_assertion
dcterms:description
"[Pursuing the hypothesis that certain unipolar and bipolar disorders may be genetically related, this study analyzed Hp genotype and allele frequencies in bipolar patients, taking into account their family history of major affective disorders.]. 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:9017976
;
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:NP703496.RAIpZYuyktdX34dM9c0WE4jxNOS9eLsPC7lmx6Vgkra4o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:07+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" .
}