@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP415825.RAgeP7ZhS-PEssPAzhhGnlaz4Qdvo-LWjX9dapWM6YFi8
> .
@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:NP415825.RAgeP7ZhS-PEssPAzhhGnlaz4Qdvo-LWjX9dapWM6YFi8130_head
{
this:
np:hasAssertion
dgn-np:NP415825.RAgeP7ZhS-PEssPAzhhGnlaz4Qdvo-LWjX9dapWM6YFi8130_assertion
;
np:hasProvenance
dgn-np:NP415825.RAgeP7ZhS-PEssPAzhhGnlaz4Qdvo-LWjX9dapWM6YFi8130_provenance
;
np:hasPublicationInfo
dgn-np:NP415825.RAgeP7ZhS-PEssPAzhhGnlaz4Qdvo-LWjX9dapWM6YFi8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP415825.RAgeP7ZhS-PEssPAzhhGnlaz4Qdvo-LWjX9dapWM6YFi8130_assertion
a
np:Assertion
.
dgn-np:NP415825.RAgeP7ZhS-PEssPAzhhGnlaz4Qdvo-LWjX9dapWM6YFi8130_provenance
a
np:Provenance
.
dgn-np:NP415825.RAgeP7ZhS-PEssPAzhhGnlaz4Qdvo-LWjX9dapWM6YFi8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP415825.RAgeP7ZhS-PEssPAzhhGnlaz4Qdvo-LWjX9dapWM6YFi8130_assertion
{
miriam-gene:6504
a
ncit:C16612
.
lld:C1868674
a
ncit:C7057
.
dgn-gda:DGN6c71a25f83675e03c14a4f277bd1a09e
sio:SIO_000628
miriam-gene:6504
,
lld:C1868674
;
a
sio:SIO_001121
.
}
dgn-np:NP415825.RAgeP7ZhS-PEssPAzhhGnlaz4Qdvo-LWjX9dapWM6YFi8130_provenance
{
dgn-np:NP415825.RAgeP7ZhS-PEssPAzhhGnlaz4Qdvo-LWjX9dapWM6YFi8130_assertion
dcterms:description
"[The gene defective in X-linked lymphoproliferative disease, SH2D1A (also named SAP or DSHP), has been identified and shown to code for an adapter protein that interacts with signaling lymphocytic activation molecule (SLAM) and several other members of the CD2 superfamily.]. 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:12629654
;
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:NP415825.RAgeP7ZhS-PEssPAzhhGnlaz4Qdvo-LWjX9dapWM6YFi8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:07+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" .
}