@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP611622.RAYbsNa1NAGwQTZYZwk47nN0PYP0vFCJp1CZyH98dZr3c
> .
@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:NP611622.RAYbsNa1NAGwQTZYZwk47nN0PYP0vFCJp1CZyH98dZr3c130_head
{
this:
np:hasAssertion
dgn-np:NP611622.RAYbsNa1NAGwQTZYZwk47nN0PYP0vFCJp1CZyH98dZr3c130_assertion
;
np:hasProvenance
dgn-np:NP611622.RAYbsNa1NAGwQTZYZwk47nN0PYP0vFCJp1CZyH98dZr3c130_provenance
;
np:hasPublicationInfo
dgn-np:NP611622.RAYbsNa1NAGwQTZYZwk47nN0PYP0vFCJp1CZyH98dZr3c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP611622.RAYbsNa1NAGwQTZYZwk47nN0PYP0vFCJp1CZyH98dZr3c130_assertion
a
np:Assertion
.
dgn-np:NP611622.RAYbsNa1NAGwQTZYZwk47nN0PYP0vFCJp1CZyH98dZr3c130_provenance
a
np:Provenance
.
dgn-np:NP611622.RAYbsNa1NAGwQTZYZwk47nN0PYP0vFCJp1CZyH98dZr3c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP611622.RAYbsNa1NAGwQTZYZwk47nN0PYP0vFCJp1CZyH98dZr3c130_assertion
{
miriam-gene:1893
a
ncit:C16612
.
lld:C0037274
a
ncit:C7057
.
dgn-gda:DGN1d3c607ee105e239f015a50a9d938f62
sio:SIO_000628
miriam-gene:1893
,
lld:C0037274
;
a
sio:SIO_001121
.
}
dgn-np:NP611622.RAYbsNa1NAGwQTZYZwk47nN0PYP0vFCJp1CZyH98dZr3c130_provenance
{
dgn-np:NP611622.RAYbsNa1NAGwQTZYZwk47nN0PYP0vFCJp1CZyH98dZr3c130_assertion
dcterms:description
"[Likewise, new clues to understanding disease pathology in lichen sclerosus have been gleaned from the discovery of pathogenic mutations in the skin protein, extracellular matrix protein 1, in the rare sclerosing inherited skin disorder, lipoid proteinosis.]. 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:15068453
;
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:NP611622.RAYbsNa1NAGwQTZYZwk47nN0PYP0vFCJp1CZyH98dZr3c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:10+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" .
}