@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP513222.RAEDaoELDqUdUNz5NiWrP4y0uHmTAjRRv5FjaPPmseZRA
> .
@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:NP513222.RAEDaoELDqUdUNz5NiWrP4y0uHmTAjRRv5FjaPPmseZRA130_head
{
this:
np:hasAssertion
dgn-np:NP513222.RAEDaoELDqUdUNz5NiWrP4y0uHmTAjRRv5FjaPPmseZRA130_assertion
;
np:hasProvenance
dgn-np:NP513222.RAEDaoELDqUdUNz5NiWrP4y0uHmTAjRRv5FjaPPmseZRA130_provenance
;
np:hasPublicationInfo
dgn-np:NP513222.RAEDaoELDqUdUNz5NiWrP4y0uHmTAjRRv5FjaPPmseZRA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP513222.RAEDaoELDqUdUNz5NiWrP4y0uHmTAjRRv5FjaPPmseZRA130_assertion
a
np:Assertion
.
dgn-np:NP513222.RAEDaoELDqUdUNz5NiWrP4y0uHmTAjRRv5FjaPPmseZRA130_provenance
a
np:Provenance
.
dgn-np:NP513222.RAEDaoELDqUdUNz5NiWrP4y0uHmTAjRRv5FjaPPmseZRA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP513222.RAEDaoELDqUdUNz5NiWrP4y0uHmTAjRRv5FjaPPmseZRA130_assertion
{
miriam-gene:3918
a
ncit:C16612
.
lld:C0079301
a
ncit:C7057
.
dgn-gda:DGNd3e5ffa7a649aa9c52ed5c408e8067c2
sio:SIO_000628
miriam-gene:3918
,
lld:C0079301
;
a
sio:SIO_001121
.
}
dgn-np:NP513222.RAEDaoELDqUdUNz5NiWrP4y0uHmTAjRRv5FjaPPmseZRA130_provenance
{
dgn-np:NP513222.RAEDaoELDqUdUNz5NiWrP4y0uHmTAjRRv5FjaPPmseZRA130_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:NP513222.RAEDaoELDqUdUNz5NiWrP4y0uHmTAjRRv5FjaPPmseZRA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:05+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" .
}