@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo
> .
@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:NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo130_head
{
this:
np:hasAssertion
dgn-np:NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo130_assertion
;
np:hasProvenance
dgn-np:NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo130_provenance
;
np:hasPublicationInfo
dgn-np:NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo130_assertion
a
np:Assertion
.
dgn-np:NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo130_provenance
a
np:Provenance
.
dgn-np:NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo130_assertion
{
miriam-gene:387715
a
ncit:C16612
.
lld:C0242383
a
ncit:C7057
.
dgn-gda:DGN0acafee43bbb765525170523b9bfc8f0
sio:SIO_000628
miriam-gene:387715
,
lld:C0242383
;
a
sio:SIO_001121
.
}
dgn-np:NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo130_provenance
{
dgn-np:NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo130_assertion
dcterms:description
"[On the basis of this and other results it is tempting to speculate that the combined effect of variants in the CFH and LOC 387715 genes may contribute to the AMD phenotype in this family.]. 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:17285240
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP592693.RANmyNa-CywBGBZXgsuT3DNW_kY977cnt3VzVJ9FUJcXo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:14+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" .
}