@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP674759.RAVKH9aN0vRk2ACLDzvr8DhoO77qyE8scpPSgIzAx5s4w
> .
@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:NP674759.RAVKH9aN0vRk2ACLDzvr8DhoO77qyE8scpPSgIzAx5s4w130_head
{
this:
np:hasAssertion
dgn-np:NP674759.RAVKH9aN0vRk2ACLDzvr8DhoO77qyE8scpPSgIzAx5s4w130_assertion
;
np:hasProvenance
dgn-np:NP674759.RAVKH9aN0vRk2ACLDzvr8DhoO77qyE8scpPSgIzAx5s4w130_provenance
;
np:hasPublicationInfo
dgn-np:NP674759.RAVKH9aN0vRk2ACLDzvr8DhoO77qyE8scpPSgIzAx5s4w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP674759.RAVKH9aN0vRk2ACLDzvr8DhoO77qyE8scpPSgIzAx5s4w130_assertion
a
np:Assertion
.
dgn-np:NP674759.RAVKH9aN0vRk2ACLDzvr8DhoO77qyE8scpPSgIzAx5s4w130_provenance
a
np:Provenance
.
dgn-np:NP674759.RAVKH9aN0vRk2ACLDzvr8DhoO77qyE8scpPSgIzAx5s4w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP674759.RAVKH9aN0vRk2ACLDzvr8DhoO77qyE8scpPSgIzAx5s4w130_assertion
{
miriam-gene:3005
a
ncit:C16612
.
lld:C0751783
a
ncit:C7057
.
dgn-gda:DGNcfbc3c4de666ecabd993931335b71b2d
sio:SIO_000628
miriam-gene:3005
,
lld:C0751783
;
a
sio:SIO_001121
.
}
dgn-np:NP674759.RAVKH9aN0vRk2ACLDzvr8DhoO77qyE8scpPSgIzAx5s4w130_provenance
{
dgn-np:NP674759.RAVKH9aN0vRk2ACLDzvr8DhoO77qyE8scpPSgIzAx5s4w130_assertion
dcterms:description
"[Modelling of the AR LBD indicate that van der Waal interactions between residue 807 (H8) to H9 and H10 were severely disrupted for the arginine mutant, but relatively preserved for the threonine and valine mutants.]. 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:11818512
;
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:NP674759.RAVKH9aN0vRk2ACLDzvr8DhoO77qyE8scpPSgIzAx5s4w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:47+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" .
}