@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ
> .
@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:NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ130_head
{
this:
np:hasAssertion
dgn-np:NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ130_assertion
;
np:hasProvenance
dgn-np:NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ130_assertion
a
np:Assertion
.
dgn-np:NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ130_provenance
a
np:Provenance
.
dgn-np:NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C1860224
a
ncit:C7057
.
dgn-gda:DGN6c0b8f0a033dc310fa44120de5ae5cd1
sio:SIO_000628
miriam-gene:4846
,
lld:C1860224
;
a
sio:SIO_001121
.
}
dgn-np:NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ130_provenance
{
dgn-np:NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ130_assertion
dcterms:description
"[We tested the hypothesis that haplotypes, as determined by tagSNPs, in NOS3 would be differentially represented in individuals with and without AMS sampled at the Janai Purnima Festival at Lake Gosain Kunda, Nepal, at 4380 m. Seven SNPs were tested, and a highly significant association (p = 0.004) was found for genotypes of the commonly studied missense polymorphism Glu298Asp (rs 1799983; G/T transversion at base 894).]. 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:19775216
;
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:NP588600.RAxCcnmIklKBpIRXDZihA7Z4u3MU-9HUdhdFZ7Q4IHSfQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:54+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" .
}