@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP930510.RA95j7cKGIDTrfmS_W45UCuFyAiTCHTRFc7gUL0NotWbU
> .
@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:NP930510.RA95j7cKGIDTrfmS_W45UCuFyAiTCHTRFc7gUL0NotWbU130_head
{
this:
np:hasAssertion
dgn-np:NP930510.RA95j7cKGIDTrfmS_W45UCuFyAiTCHTRFc7gUL0NotWbU130_assertion
;
np:hasProvenance
dgn-np:NP930510.RA95j7cKGIDTrfmS_W45UCuFyAiTCHTRFc7gUL0NotWbU130_provenance
;
np:hasPublicationInfo
dgn-np:NP930510.RA95j7cKGIDTrfmS_W45UCuFyAiTCHTRFc7gUL0NotWbU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP930510.RA95j7cKGIDTrfmS_W45UCuFyAiTCHTRFc7gUL0NotWbU130_assertion
a
np:Assertion
.
dgn-np:NP930510.RA95j7cKGIDTrfmS_W45UCuFyAiTCHTRFc7gUL0NotWbU130_provenance
a
np:Provenance
.
dgn-np:NP930510.RA95j7cKGIDTrfmS_W45UCuFyAiTCHTRFc7gUL0NotWbU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP930510.RA95j7cKGIDTrfmS_W45UCuFyAiTCHTRFc7gUL0NotWbU130_assertion
{
miriam-gene:4312
a
ncit:C16612
.
lld:C0079474
a
ncit:C7057
.
dgn-gda:DGNc9a83fc52b00f7be18a8bd9a6613fb30
sio:SIO_000628
miriam-gene:4312
,
lld:C0079474
;
a
sio:SIO_001121
.
}
dgn-np:NP930510.RA95j7cKGIDTrfmS_W45UCuFyAiTCHTRFc7gUL0NotWbU130_provenance
{
dgn-np:NP930510.RA95j7cKGIDTrfmS_W45UCuFyAiTCHTRFc7gUL0NotWbU130_assertion
dcterms:description
"[Recently, the MMP1 promoter single nucleotide polymorphism (SNP) rs1799750, designated as 1G 2G, was shown to be involved in modulation of disease severity in patients with recessive DEB (RDEB), and was proposed as a genetic modifier.]. 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:19681861
;
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:NP930510.RA95j7cKGIDTrfmS_W45UCuFyAiTCHTRFc7gUL0NotWbU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:30+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" .
}