@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP640078.RAeyUoy4EIzbUm-CFcLFJIkdSHdEuuGT0fm_qyUB9Pq5g
> .
@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:NP640078.RAeyUoy4EIzbUm-CFcLFJIkdSHdEuuGT0fm_qyUB9Pq5g130_head
{
this:
np:hasAssertion
dgn-np:NP640078.RAeyUoy4EIzbUm-CFcLFJIkdSHdEuuGT0fm_qyUB9Pq5g130_assertion
;
np:hasProvenance
dgn-np:NP640078.RAeyUoy4EIzbUm-CFcLFJIkdSHdEuuGT0fm_qyUB9Pq5g130_provenance
;
np:hasPublicationInfo
dgn-np:NP640078.RAeyUoy4EIzbUm-CFcLFJIkdSHdEuuGT0fm_qyUB9Pq5g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP640078.RAeyUoy4EIzbUm-CFcLFJIkdSHdEuuGT0fm_qyUB9Pq5g130_assertion
a
np:Assertion
.
dgn-np:NP640078.RAeyUoy4EIzbUm-CFcLFJIkdSHdEuuGT0fm_qyUB9Pq5g130_provenance
a
np:Provenance
.
dgn-np:NP640078.RAeyUoy4EIzbUm-CFcLFJIkdSHdEuuGT0fm_qyUB9Pq5g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP640078.RAeyUoy4EIzbUm-CFcLFJIkdSHdEuuGT0fm_qyUB9Pq5g130_assertion
{
miriam-gene:6736
a
ncit:C16612
.
lld:C0011119
a
ncit:C7057
.
dgn-gda:DGN92511d6f1ae91483c2d1e3f8b57f840e
sio:SIO_000628
miriam-gene:6736
,
lld:C0011119
;
a
sio:SIO_001121
.
}
dgn-np:NP640078.RAeyUoy4EIzbUm-CFcLFJIkdSHdEuuGT0fm_qyUB9Pq5g130_provenance
{
dgn-np:NP640078.RAeyUoy4EIzbUm-CFcLFJIkdSHdEuuGT0fm_qyUB9Pq5g130_assertion
dcterms:description
"[Our results (i) identify a shared SRY-DNA contact at a site of either induced or intrinsic DNA bending, (ii) demonstrate that this contact is not required to bind an intrinsically bent DNA target, and (iii) rationalize patterns of sequence conservation or diversity among HMG boxes.]. 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:7718558
;
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:NP640078.RAeyUoy4EIzbUm-CFcLFJIkdSHdEuuGT0fm_qyUB9Pq5g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:26+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" .
}