@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP138159.RAjp-ywyM8lziizNsbTY-M0ZZbVZw0wlpbpi7hfiypS-Y
> .
@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:NP138159.RAjp-ywyM8lziizNsbTY-M0ZZbVZw0wlpbpi7hfiypS-Y130_head
{
this:
np:hasAssertion
dgn-np:NP138159.RAjp-ywyM8lziizNsbTY-M0ZZbVZw0wlpbpi7hfiypS-Y130_assertion
;
np:hasProvenance
dgn-np:NP138159.RAjp-ywyM8lziizNsbTY-M0ZZbVZw0wlpbpi7hfiypS-Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP138159.RAjp-ywyM8lziizNsbTY-M0ZZbVZw0wlpbpi7hfiypS-Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP138159.RAjp-ywyM8lziizNsbTY-M0ZZbVZw0wlpbpi7hfiypS-Y130_assertion
a
np:Assertion
.
dgn-np:NP138159.RAjp-ywyM8lziizNsbTY-M0ZZbVZw0wlpbpi7hfiypS-Y130_provenance
a
np:Provenance
.
dgn-np:NP138159.RAjp-ywyM8lziizNsbTY-M0ZZbVZw0wlpbpi7hfiypS-Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP138159.RAjp-ywyM8lziizNsbTY-M0ZZbVZw0wlpbpi7hfiypS-Y130_assertion
{
miriam-gene:3075
a
ncit:C16612
.
lld:C0242383
a
ncit:C7057
.
dgn-gda:DGN515ecb77bd96545be85d8a03dc1088b2
sio:SIO_000628
miriam-gene:3075
,
lld:C0242383
;
a
sio:SIO_001121
.
}
dgn-np:NP138159.RAjp-ywyM8lziizNsbTY-M0ZZbVZw0wlpbpi7hfiypS-Y130_provenance
{
dgn-np:NP138159.RAjp-ywyM8lziizNsbTY-M0ZZbVZw0wlpbpi7hfiypS-Y130_assertion
dcterms:description
"[findings are consistent with evidence that, in addition to the widely described Y402H variant, there is at least one and, most probably, several other mutations in the CFH gene which determine disease manifestation in age-related macular degeneration ]. 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:17314151
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP138159.RAjp-ywyM8lziizNsbTY-M0ZZbVZw0wlpbpi7hfiypS-Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:12+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" .
}