@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP74046.RApeNHsMB90ZqG7kqX1szbx4SjcUYQQ2L3mD1rMdLnkLM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP74046.RApeNHsMB90ZqG7kqX1szbx4SjcUYQQ2L3mD1rMdLnkLM130_head
{
this:
np:hasAssertion
dgn-np:NP74046.RApeNHsMB90ZqG7kqX1szbx4SjcUYQQ2L3mD1rMdLnkLM130_assertion
;
np:hasProvenance
dgn-np:NP74046.RApeNHsMB90ZqG7kqX1szbx4SjcUYQQ2L3mD1rMdLnkLM130_provenance
;
np:hasPublicationInfo
dgn-np:NP74046.RApeNHsMB90ZqG7kqX1szbx4SjcUYQQ2L3mD1rMdLnkLM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP74046.RApeNHsMB90ZqG7kqX1szbx4SjcUYQQ2L3mD1rMdLnkLM130_assertion
a
np:Assertion
.
dgn-np:NP74046.RApeNHsMB90ZqG7kqX1szbx4SjcUYQQ2L3mD1rMdLnkLM130_provenance
a
np:Provenance
.
dgn-np:NP74046.RApeNHsMB90ZqG7kqX1szbx4SjcUYQQ2L3mD1rMdLnkLM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP74046.RApeNHsMB90ZqG7kqX1szbx4SjcUYQQ2L3mD1rMdLnkLM130_assertion
{
miriam-gene:4653
a
ncit:C16612
.
lld:C0017601
a
ncit:C7057
.
dgn-gda:DGN4156e3cb74634800307bbe85de7a8656
sio:SIO_000628
miriam-gene:4653
,
lld:C0017601
;
a
sio:SIO_001122
.
}
dgn-np:NP74046.RApeNHsMB90ZqG7kqX1szbx4SjcUYQQ2L3mD1rMdLnkLM130_provenance
{
dgn-np:NP74046.RApeNHsMB90ZqG7kqX1szbx4SjcUYQQ2L3mD1rMdLnkLM130_assertion
dcterms:description
"[ Since the Asp 208 Glu mutation was found in NTG, the pathogenesis of glaucoma with myocilin mutation might be more complex and it may be related to weakness of the optic nerve head. On the other hand, the mutation may be a polymorphism. The Ile 360 Asn m]. 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:11979979
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP74046.RApeNHsMB90ZqG7kqX1szbx4SjcUYQQ2L3mD1rMdLnkLM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:21+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}