@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP166117.RAXrce6a8vmTYAKYllg6h25aNass9uuhlXepP1uYUfYIY
> .
@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:NP166117.RAXrce6a8vmTYAKYllg6h25aNass9uuhlXepP1uYUfYIY130_head
{
this:
np:hasAssertion
dgn-np:NP166117.RAXrce6a8vmTYAKYllg6h25aNass9uuhlXepP1uYUfYIY130_assertion
;
np:hasProvenance
dgn-np:NP166117.RAXrce6a8vmTYAKYllg6h25aNass9uuhlXepP1uYUfYIY130_provenance
;
np:hasPublicationInfo
dgn-np:NP166117.RAXrce6a8vmTYAKYllg6h25aNass9uuhlXepP1uYUfYIY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP166117.RAXrce6a8vmTYAKYllg6h25aNass9uuhlXepP1uYUfYIY130_assertion
a
np:Assertion
.
dgn-np:NP166117.RAXrce6a8vmTYAKYllg6h25aNass9uuhlXepP1uYUfYIY130_provenance
a
np:Provenance
.
dgn-np:NP166117.RAXrce6a8vmTYAKYllg6h25aNass9uuhlXepP1uYUfYIY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP166117.RAXrce6a8vmTYAKYllg6h25aNass9uuhlXepP1uYUfYIY130_assertion
{
miriam-gene:6653
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN94b878e774c2e9e75037e1f5c28e494d
sio:SIO_000628
miriam-gene:6653
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP166117.RAXrce6a8vmTYAKYllg6h25aNass9uuhlXepP1uYUfYIY130_provenance
{
dgn-np:NP166117.RAXrce6a8vmTYAKYllg6h25aNass9uuhlXepP1uYUfYIY130_assertion
dcterms:description
"[These data are consistent with either allelic heterogeneity or the existence of as yet untested functional variants and these will be important considerations in further attempts to evaluate the importance of sequence variation in SORL1 with AD risk.]. 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:19653016
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP166117.RAXrce6a8vmTYAKYllg6h25aNass9uuhlXepP1uYUfYIY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:30+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" .
}