@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8
> .
@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:NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8130_head
{
this:
np:hasAssertion
dgn-np:NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8130_assertion
;
np:hasProvenance
dgn-np:NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8130_provenance
;
np:hasPublicationInfo
dgn-np:NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8130_assertion
a
np:Assertion
.
dgn-np:NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8130_provenance
a
np:Provenance
.
dgn-np:NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8130_assertion
{
miriam-gene:154
a
ncit:C16612
.
lld:C0039494
a
ncit:C7057
.
dgn-gda:DGN08d7168e93e3eb95d7aec29448ef0d79
sio:SIO_000628
miriam-gene:154
,
lld:C0039494
;
a
sio:SIO_001121
.
}
dgn-np:NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8130_provenance
{
dgn-np:NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8130_assertion
dcterms:description
"[Individuals who carried one haplotype coding for high and one coding for low ADRB2 expression displayed the highest positive psychological traits, had higher levels of resting arterial pressure, and were about 10 times less likely to develop TMD.]. 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:16741943
;
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:NP603536.RADqMskfuRSnin0rG-1qebX58pGLjH9Yx6EhUniUHkrn8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:02+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" .
}