@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP744540.RAVLYR79bjs97lM53IRxAi8CgV2MP8I3wfOGHRe_nV7Fc
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP744540.RAVLYR79bjs97lM53IRxAi8CgV2MP8I3wfOGHRe_nV7Fc130_head
{
this:
np:hasAssertion
dgn-np:NP744540.RAVLYR79bjs97lM53IRxAi8CgV2MP8I3wfOGHRe_nV7Fc130_assertion
;
np:hasProvenance
dgn-np:NP744540.RAVLYR79bjs97lM53IRxAi8CgV2MP8I3wfOGHRe_nV7Fc130_provenance
;
np:hasPublicationInfo
dgn-np:NP744540.RAVLYR79bjs97lM53IRxAi8CgV2MP8I3wfOGHRe_nV7Fc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP744540.RAVLYR79bjs97lM53IRxAi8CgV2MP8I3wfOGHRe_nV7Fc130_assertion
a
np:Assertion
.
dgn-np:NP744540.RAVLYR79bjs97lM53IRxAi8CgV2MP8I3wfOGHRe_nV7Fc130_provenance
a
np:Provenance
.
dgn-np:NP744540.RAVLYR79bjs97lM53IRxAi8CgV2MP8I3wfOGHRe_nV7Fc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP744540.RAVLYR79bjs97lM53IRxAi8CgV2MP8I3wfOGHRe_nV7Fc130_assertion
{
miriam-gene:578
a
ncit:C16612
.
lld:C0003486
a
ncit:C7057
.
dgn-gda:DGN70545efda70c952c708642ecb18c8d6d
sio:SIO_000628
miriam-gene:578
,
lld:C0003486
;
a
sio:SIO_001121
.
}
dgn-np:NP744540.RAVLYR79bjs97lM53IRxAi8CgV2MP8I3wfOGHRe_nV7Fc130_provenance
{
dgn-np:NP744540.RAVLYR79bjs97lM53IRxAi8CgV2MP8I3wfOGHRe_nV7Fc130_assertion
dcterms:description
"[Therefore, the fact that different BAK1 variants can exist in both diseased and nondiseased AA tissues compared to matching blood samples, together with the rare occurrence of these same SNPs in reference sequences, suggests that selection may be a significant factor in AAA ontogeny.]. 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:19514060
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP744540.RAVLYR79bjs97lM53IRxAi8CgV2MP8I3wfOGHRe_nV7Fc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:22+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}