@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU
> .
@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:NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_head
{
this:
np:hasAssertion
dgn-np:NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_assertion
;
np:hasProvenance
dgn-np:NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_provenance
;
np:hasPublicationInfo
dgn-np:NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_assertion
a
np:Assertion
.
dgn-np:NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_provenance
a
np:Provenance
.
dgn-np:NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_assertion
{
miriam-gene:63943
a
ncit:C16612
.
lld:C0242383
a
ncit:C7057
.
dgn-gda:DGN0b85c21292148ef1e6ae8d7372b9aa39
sio:SIO_000628
miriam-gene:63943
,
lld:C0242383
;
a
sio:SIO_001122
.
}
dgn-np:NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_provenance
{
dgn-np:NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_assertion
dcterms:description
"[TNXB, FKBPL and NOTCH4 are all plausible AMD susceptibility genes, but further research will be needed to identify the causal variants and determine whether any of these genes are involved in the pathogenesis of AMD.]. 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:22694956
;
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:NP936362.RA-eNQXPqDluOGAbcjOTFSHQkih76ALh2m0qWu4rqEaPU130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:12+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: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" .
}