@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP175831.RAErZJPUAQWaypWFpPge_FyewdYWJM4LGy5xjDtf7hmzk
> .
@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:NP175831.RAErZJPUAQWaypWFpPge_FyewdYWJM4LGy5xjDtf7hmzk130_head
{
this:
np:hasAssertion
dgn-np:NP175831.RAErZJPUAQWaypWFpPge_FyewdYWJM4LGy5xjDtf7hmzk130_assertion
;
np:hasProvenance
dgn-np:NP175831.RAErZJPUAQWaypWFpPge_FyewdYWJM4LGy5xjDtf7hmzk130_provenance
;
np:hasPublicationInfo
dgn-np:NP175831.RAErZJPUAQWaypWFpPge_FyewdYWJM4LGy5xjDtf7hmzk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP175831.RAErZJPUAQWaypWFpPge_FyewdYWJM4LGy5xjDtf7hmzk130_assertion
a
np:Assertion
.
dgn-np:NP175831.RAErZJPUAQWaypWFpPge_FyewdYWJM4LGy5xjDtf7hmzk130_provenance
a
np:Provenance
.
dgn-np:NP175831.RAErZJPUAQWaypWFpPge_FyewdYWJM4LGy5xjDtf7hmzk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP175831.RAErZJPUAQWaypWFpPge_FyewdYWJM4LGy5xjDtf7hmzk130_assertion
{
miriam-gene:3913
a
ncit:C16612
.
lld:C1836876
a
ncit:C7057
.
dgn-gda:DGN72dc2197269c91353d766e6fde95474b
sio:SIO_000628
miriam-gene:3913
,
lld:C1836876
;
a
sio:SIO_001121
.
}
dgn-np:NP175831.RAErZJPUAQWaypWFpPge_FyewdYWJM4LGy5xjDtf7hmzk130_provenance
{
dgn-np:NP175831.RAErZJPUAQWaypWFpPge_FyewdYWJM4LGy5xjDtf7hmzk130_assertion
dcterms:description
"[Genetic diseases affecting laminin and type IV collagen synthesis also are presented, with an emphasis on mutations to LAMB2 (Pierson syndrome) and COL4A3, COL4A4, and COL4A5 (Alport syndrome), and their experimental mouse models.]. 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:22958488
;
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:NP175831.RAErZJPUAQWaypWFpPge_FyewdYWJM4LGy5xjDtf7hmzk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:35+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" .
}