@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP781835.RAhKhkbxLAPcilJYf8v_4n8iX5lN5FgUrXxxoUYIXf4bs
> .
@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:NP781835.RAhKhkbxLAPcilJYf8v_4n8iX5lN5FgUrXxxoUYIXf4bs130_head
{
this:
np:hasAssertion
dgn-np:NP781835.RAhKhkbxLAPcilJYf8v_4n8iX5lN5FgUrXxxoUYIXf4bs130_assertion
;
np:hasProvenance
dgn-np:NP781835.RAhKhkbxLAPcilJYf8v_4n8iX5lN5FgUrXxxoUYIXf4bs130_provenance
;
np:hasPublicationInfo
dgn-np:NP781835.RAhKhkbxLAPcilJYf8v_4n8iX5lN5FgUrXxxoUYIXf4bs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP781835.RAhKhkbxLAPcilJYf8v_4n8iX5lN5FgUrXxxoUYIXf4bs130_assertion
a
np:Assertion
.
dgn-np:NP781835.RAhKhkbxLAPcilJYf8v_4n8iX5lN5FgUrXxxoUYIXf4bs130_provenance
a
np:Provenance
.
dgn-np:NP781835.RAhKhkbxLAPcilJYf8v_4n8iX5lN5FgUrXxxoUYIXf4bs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP781835.RAhKhkbxLAPcilJYf8v_4n8iX5lN5FgUrXxxoUYIXf4bs130_assertion
{
miriam-gene:3161
a
ncit:C16612
.
lld:C1336076
a
ncit:C7057
.
dgn-gda:DGNf789c84ac848f16b608b7044edd971b4
sio:SIO_000628
miriam-gene:3161
,
lld:C1336076
;
a
sio:SIO_001121
.
}
dgn-np:NP781835.RAhKhkbxLAPcilJYf8v_4n8iX5lN5FgUrXxxoUYIXf4bs130_provenance
{
dgn-np:NP781835.RAhKhkbxLAPcilJYf8v_4n8iX5lN5FgUrXxxoUYIXf4bs130_assertion
dcterms:description
"[Taken together, our data provide fundamental insight into apicobasal polarization through BRCA1 function, which may explain the expanded cell subsets and characteristic tumor type accompanying BRCA1 mutation, while also linking this process to sporadic breast cancer through perturbation of HMMR/RHAMM.]. 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:22110403
;
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:NP781835.RAhKhkbxLAPcilJYf8v_4n8iX5lN5FgUrXxxoUYIXf4bs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:53+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" .
}