@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac
> .
@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:NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac130_head
{
this:
np:hasAssertion
dgn-np:NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac130_assertion
;
np:hasProvenance
dgn-np:NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac130_provenance
;
np:hasPublicationInfo
dgn-np:NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac130_assertion
a
np:Assertion
.
dgn-np:NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac130_provenance
a
np:Provenance
.
dgn-np:NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac130_assertion
{
miriam-gene:6976
a
ncit:C16612
.
lld:C0004364
a
ncit:C7057
.
dgn-gda:DGN5e710b50cb526cb819dcc579f119c053
sio:SIO_000628
miriam-gene:6976
,
lld:C0004364
;
a
sio:SIO_001121
.
}
dgn-np:NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac130_provenance
{
dgn-np:NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac130_assertion
dcterms:description
"[Polymorphisms in T-cell receptor genes can provide important information for the study of the immune response and autoimmune diseases; indeed, rs1800907, a very common single nucleotide polymorphism (SNP) of the TCRB, has been extensively studied in autoimmune diseases in the 1990s using Southern blot analysis and more recently polymerase chain reaction (PCR) and sequencing.]. 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:21599810
;
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:NP482882.RAwkHVpHE7lXwfH28WwoaS0IY7pSlW9xHwv3P7dooJpac130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:49+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" .
}