@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP235648.RAAheW2abw-NkdR4QOGZWU3tRUzHf5iBPr5yJQNRhijiQ
> .
@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:NP235648.RAAheW2abw-NkdR4QOGZWU3tRUzHf5iBPr5yJQNRhijiQ130_head
{
this:
np:hasAssertion
dgn-np:NP235648.RAAheW2abw-NkdR4QOGZWU3tRUzHf5iBPr5yJQNRhijiQ130_assertion
;
np:hasProvenance
dgn-np:NP235648.RAAheW2abw-NkdR4QOGZWU3tRUzHf5iBPr5yJQNRhijiQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP235648.RAAheW2abw-NkdR4QOGZWU3tRUzHf5iBPr5yJQNRhijiQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP235648.RAAheW2abw-NkdR4QOGZWU3tRUzHf5iBPr5yJQNRhijiQ130_assertion
a
np:Assertion
.
dgn-np:NP235648.RAAheW2abw-NkdR4QOGZWU3tRUzHf5iBPr5yJQNRhijiQ130_provenance
a
np:Provenance
.
dgn-np:NP235648.RAAheW2abw-NkdR4QOGZWU3tRUzHf5iBPr5yJQNRhijiQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP235648.RAAheW2abw-NkdR4QOGZWU3tRUzHf5iBPr5yJQNRhijiQ130_assertion
{
miriam-gene:7433
a
ncit:C16612
.
lld:C0038644
a
ncit:C7057
.
dgn-gda:DGNb28854435d5d6dff48fcec340a78816c
sio:SIO_000628
miriam-gene:7433
,
lld:C0038644
;
a
sio:SIO_001121
.
}
dgn-np:NP235648.RAAheW2abw-NkdR4QOGZWU3tRUzHf5iBPr5yJQNRhijiQ130_provenance
{
dgn-np:NP235648.RAAheW2abw-NkdR4QOGZWU3tRUzHf5iBPr5yJQNRhijiQ130_assertion
dcterms:description
"[To investigate whether all substitutions in the first hypervariable region (HVR1) in sudden infant death syndrome (SIDS) can be recovered along the maternal line of the family (inherited), or whether SIDS victims have new substitutions compared to maternal relatives (somatic mutations) that may be related to environmental factors.]. 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:12434891
;
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:NP235648.RAAheW2abw-NkdR4QOGZWU3tRUzHf5iBPr5yJQNRhijiQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:12+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" .
}