@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP446645.RASC15mt7p83bSh6TPtJqrmka2-bJIauDi7fUmwpxMd1k
> .
@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/v3.0.0/void/
> .
dgn-np:NP446645.RASC15mt7p83bSh6TPtJqrmka2-bJIauDi7fUmwpxMd1k130_head
{
this:
np:hasAssertion
dgn-np:NP446645.RASC15mt7p83bSh6TPtJqrmka2-bJIauDi7fUmwpxMd1k130_assertion
;
np:hasProvenance
dgn-np:NP446645.RASC15mt7p83bSh6TPtJqrmka2-bJIauDi7fUmwpxMd1k130_provenance
;
np:hasPublicationInfo
dgn-np:NP446645.RASC15mt7p83bSh6TPtJqrmka2-bJIauDi7fUmwpxMd1k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP446645.RASC15mt7p83bSh6TPtJqrmka2-bJIauDi7fUmwpxMd1k130_assertion
a
np:Assertion
.
dgn-np:NP446645.RASC15mt7p83bSh6TPtJqrmka2-bJIauDi7fUmwpxMd1k130_provenance
a
np:Provenance
.
dgn-np:NP446645.RASC15mt7p83bSh6TPtJqrmka2-bJIauDi7fUmwpxMd1k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP446645.RASC15mt7p83bSh6TPtJqrmka2-bJIauDi7fUmwpxMd1k130_assertion
{
miriam-gene:3075
a
ncit:C16612
.
lld:C3665346
a
ncit:C7057
.
dgn-gda:DGN167d56227e8a2c0310ef52339929d27c
sio:SIO_000628
miriam-gene:3075
,
lld:C3665346
;
a
sio:SIO_001121
.
}
dgn-np:NP446645.RASC15mt7p83bSh6TPtJqrmka2-bJIauDi7fUmwpxMd1k130_provenance
{
dgn-np:NP446645.RASC15mt7p83bSh6TPtJqrmka2-bJIauDi7fUmwpxMd1k130_assertion
dcterms:description
"[Our findings strongly suggest that monogenic inheritance of CFH variants can result in basal laminar drusen in young adults, and this can progress to maculopathy and severe vision loss later in life.]. 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:18252232
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP446645.RASC15mt7p83bSh6TPtJqrmka2-bJIauDi7fUmwpxMd1k130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:01+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}