@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48483.RAj4R4HyfHtfe2-PkwuPbGFQY7AHV-E6Scm_Gc_baISL4
> .
@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 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:NP48483.RAj4R4HyfHtfe2-PkwuPbGFQY7AHV-E6Scm_Gc_baISL4130_head
{
this:
np:hasAssertion
dgn-np:NP48483.RAj4R4HyfHtfe2-PkwuPbGFQY7AHV-E6Scm_Gc_baISL4130_assertion
;
np:hasProvenance
dgn-np:NP48483.RAj4R4HyfHtfe2-PkwuPbGFQY7AHV-E6Scm_Gc_baISL4130_provenance
;
np:hasPublicationInfo
dgn-np:NP48483.RAj4R4HyfHtfe2-PkwuPbGFQY7AHV-E6Scm_Gc_baISL4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48483.RAj4R4HyfHtfe2-PkwuPbGFQY7AHV-E6Scm_Gc_baISL4130_assertion
a
np:Assertion
.
dgn-np:NP48483.RAj4R4HyfHtfe2-PkwuPbGFQY7AHV-E6Scm_Gc_baISL4130_provenance
a
np:Provenance
.
dgn-np:NP48483.RAj4R4HyfHtfe2-PkwuPbGFQY7AHV-E6Scm_Gc_baISL4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48483.RAj4R4HyfHtfe2-PkwuPbGFQY7AHV-E6Scm_Gc_baISL4130_assertion
{
miriam-gene:335
a
ncit:C16612
.
lld:C0020473
a
ncit:C7057
.
dgn-gda:DGN528d4c057ad73faa533d1370866ba06a
sio:SIO_000628
miriam-gene:335
,
lld:C0020473
;
a
sio:SIO_001122
.
}
dgn-np:NP48483.RAj4R4HyfHtfe2-PkwuPbGFQY7AHV-E6Scm_Gc_baISL4130_provenance
{
dgn-np:NP48483.RAj4R4HyfHtfe2-PkwuPbGFQY7AHV-E6Scm_Gc_baISL4130_assertion
dct:description
"[While these effects can be attributed to the presence of the M2 and S2 minor alleles, these results suggest that the importance of specific allelic haplotypes may be greater than single genotypic effects.]. 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:11181747
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP48483.RAj4R4HyfHtfe2-PkwuPbGFQY7AHV-E6Scm_Gc_baISL4130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:22+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}