@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP754386.RAUMsSB7F6RMuzIoNleXQK5EwX3NHunIdOCoUkLrXlpMw
> .
@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:NP754386.RAUMsSB7F6RMuzIoNleXQK5EwX3NHunIdOCoUkLrXlpMw130_head
{
this:
np:hasAssertion
dgn-np:NP754386.RAUMsSB7F6RMuzIoNleXQK5EwX3NHunIdOCoUkLrXlpMw130_assertion
;
np:hasProvenance
dgn-np:NP754386.RAUMsSB7F6RMuzIoNleXQK5EwX3NHunIdOCoUkLrXlpMw130_provenance
;
np:hasPublicationInfo
dgn-np:NP754386.RAUMsSB7F6RMuzIoNleXQK5EwX3NHunIdOCoUkLrXlpMw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP754386.RAUMsSB7F6RMuzIoNleXQK5EwX3NHunIdOCoUkLrXlpMw130_assertion
a
np:Assertion
.
dgn-np:NP754386.RAUMsSB7F6RMuzIoNleXQK5EwX3NHunIdOCoUkLrXlpMw130_provenance
a
np:Provenance
.
dgn-np:NP754386.RAUMsSB7F6RMuzIoNleXQK5EwX3NHunIdOCoUkLrXlpMw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP754386.RAUMsSB7F6RMuzIoNleXQK5EwX3NHunIdOCoUkLrXlpMw130_assertion
{
miriam-gene:3909
a
ncit:C16612
.
lld:C0037274
a
ncit:C7057
.
dgn-gda:DGNee370af42c04d1ce807b2935654c00dc
sio:SIO_000628
miriam-gene:3909
,
lld:C0037274
;
a
sio:SIO_001121
.
}
dgn-np:NP754386.RAUMsSB7F6RMuzIoNleXQK5EwX3NHunIdOCoUkLrXlpMw130_provenance
{
dgn-np:NP754386.RAUMsSB7F6RMuzIoNleXQK5EwX3NHunIdOCoUkLrXlpMw130_assertion
dcterms:description
"[The three genes (LAMA3, LAB3 and LAMC2) that encode the anchoring filament protein, laminin 5, may all harbour pathogenetic mutations in the autosomal recessive blistering skin disorder, junctional epidermolysis bullosa (JEB).]. 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:9205497
;
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:NP754386.RAUMsSB7F6RMuzIoNleXQK5EwX3NHunIdOCoUkLrXlpMw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:37+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" .
}