@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP711021.RAmPvBH9JC3qo5as9pspfarvb74e5eM9ze1bQmvv8W17s
> .
@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:NP711021.RAmPvBH9JC3qo5as9pspfarvb74e5eM9ze1bQmvv8W17s130_head
{
this:
np:hasAssertion
dgn-np:NP711021.RAmPvBH9JC3qo5as9pspfarvb74e5eM9ze1bQmvv8W17s130_assertion
;
np:hasProvenance
dgn-np:NP711021.RAmPvBH9JC3qo5as9pspfarvb74e5eM9ze1bQmvv8W17s130_provenance
;
np:hasPublicationInfo
dgn-np:NP711021.RAmPvBH9JC3qo5as9pspfarvb74e5eM9ze1bQmvv8W17s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP711021.RAmPvBH9JC3qo5as9pspfarvb74e5eM9ze1bQmvv8W17s130_assertion
a
np:Assertion
.
dgn-np:NP711021.RAmPvBH9JC3qo5as9pspfarvb74e5eM9ze1bQmvv8W17s130_provenance
a
np:Provenance
.
dgn-np:NP711021.RAmPvBH9JC3qo5as9pspfarvb74e5eM9ze1bQmvv8W17s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP711021.RAmPvBH9JC3qo5as9pspfarvb74e5eM9ze1bQmvv8W17s130_assertion
{
miriam-gene:3133
a
ncit:C16612
.
lld:C0270814
a
ncit:C7057
.
dgn-gda:DGN6073c90dd53eeee2b2af749f74cea5ab
sio:SIO_000628
miriam-gene:3133
,
lld:C0270814
;
a
sio:SIO_001121
.
}
dgn-np:NP711021.RAmPvBH9JC3qo5as9pspfarvb74e5eM9ze1bQmvv8W17s130_provenance
{
dgn-np:NP711021.RAmPvBH9JC3qo5as9pspfarvb74e5eM9ze1bQmvv8W17s130_assertion
dcterms:description
"[The problem of understanding the meaning of the association of susceptibility with diverse MHC alleles such as DR4 (Dw4 and Dw14), DR1, and DRw10 is approached by detailed biochemical analysis that led to the identification of common stretches of amino acid sequence, presumably encoding conformationally equivalent structures.]. 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:3142068
;
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:NP711021.RAmPvBH9JC3qo5as9pspfarvb74e5eM9ze1bQmvv8W17s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:12+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" .
}