@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP289108.RAYzeOSAAp67ePpkDum0MoCiAJQSSwgIU5tWxYAzwGXgs
> .
@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:NP289108.RAYzeOSAAp67ePpkDum0MoCiAJQSSwgIU5tWxYAzwGXgs130_head
{
this:
np:hasAssertion
dgn-np:NP289108.RAYzeOSAAp67ePpkDum0MoCiAJQSSwgIU5tWxYAzwGXgs130_assertion
;
np:hasProvenance
dgn-np:NP289108.RAYzeOSAAp67ePpkDum0MoCiAJQSSwgIU5tWxYAzwGXgs130_provenance
;
np:hasPublicationInfo
dgn-np:NP289108.RAYzeOSAAp67ePpkDum0MoCiAJQSSwgIU5tWxYAzwGXgs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP289108.RAYzeOSAAp67ePpkDum0MoCiAJQSSwgIU5tWxYAzwGXgs130_assertion
a
np:Assertion
.
dgn-np:NP289108.RAYzeOSAAp67ePpkDum0MoCiAJQSSwgIU5tWxYAzwGXgs130_provenance
a
np:Provenance
.
dgn-np:NP289108.RAYzeOSAAp67ePpkDum0MoCiAJQSSwgIU5tWxYAzwGXgs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP289108.RAYzeOSAAp67ePpkDum0MoCiAJQSSwgIU5tWxYAzwGXgs130_assertion
{
miriam-gene:4313
a
ncit:C16612
.
lld:C0162871
a
ncit:C7057
.
dgn-gda:DGN2047610e014ae2212e44ca7f1390d5c1
sio:SIO_000628
miriam-gene:4313
,
lld:C0162871
;
a
sio:SIO_001121
.
}
dgn-np:NP289108.RAYzeOSAAp67ePpkDum0MoCiAJQSSwgIU5tWxYAzwGXgs130_provenance
{
dgn-np:NP289108.RAYzeOSAAp67ePpkDum0MoCiAJQSSwgIU5tWxYAzwGXgs130_assertion
dcterms:description
"[Our analysis of the entire coding region and three parts of the promoter of the MMP2 gene failed to show an association between genetic polymorphisms and AAA, suggesting that variations in the MMP2 gene do not contribute to the development of AAA.]. 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:16458924
;
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:NP289108.RAYzeOSAAp67ePpkDum0MoCiAJQSSwgIU5tWxYAzwGXgs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:44+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" .
}