@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8
> .
@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:NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8130_head
{
this:
np:hasAssertion
dgn-np:NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8130_assertion
;
np:hasProvenance
dgn-np:NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8130_provenance
;
np:hasPublicationInfo
dgn-np:NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8130_assertion
a
np:Assertion
.
dgn-np:NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8130_provenance
a
np:Provenance
.
dgn-np:NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8130_assertion
{
miriam-gene:8856
a
ncit:C16612
.
lld:C0751783
a
ncit:C7057
.
dgn-gda:DGN558085ce6c15d6957974110ddde3a7e4
sio:SIO_000628
miriam-gene:8856
,
lld:C0751783
;
a
sio:SIO_001121
.
}
dgn-np:NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8130_provenance
{
dgn-np:NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8130_assertion
dcterms:description
"[The most abundant PXR alternative mRNA transcripts lacked 111 nucleotides, deleting 37 amino acids from the PXR LBD (PXR.2), or lacked 123 nt, deleting 41 amino acids from the PXR LBD (PXR.3).]. 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:15364541
;
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:NP440590.RAcn2I6FR7TbPxaIOOBibdwDfTcbuSYBcY3BK1Iq4xnP8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:20+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" .
}