@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP271075.RAJdaPhCu-z6EmnIz__NIyUpoIoPWkfdeO_F2lPR68Ng8
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP271075.RAJdaPhCu-z6EmnIz__NIyUpoIoPWkfdeO_F2lPR68Ng8130_head
{
this:
np:hasAssertion
dgn-np:NP271075.RAJdaPhCu-z6EmnIz__NIyUpoIoPWkfdeO_F2lPR68Ng8130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP271075.RAJdaPhCu-z6EmnIz__NIyUpoIoPWkfdeO_F2lPR68Ng8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP271075.RAJdaPhCu-z6EmnIz__NIyUpoIoPWkfdeO_F2lPR68Ng8130_assertion
a
np:Assertion
.
dgn-np:NP271075.RAJdaPhCu-z6EmnIz__NIyUpoIoPWkfdeO_F2lPR68Ng8130_provenance
a
np:Provenance
.
dgn-np:NP271075.RAJdaPhCu-z6EmnIz__NIyUpoIoPWkfdeO_F2lPR68Ng8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP271075.RAJdaPhCu-z6EmnIz__NIyUpoIoPWkfdeO_F2lPR68Ng8130_assertion
{
miriam-gene:695
a
ncit:C16612
.
lld:C0221026
a
ncit:C7057
.
dgn-gda:DGNb357b58593f7a3542af999ac26db0bef
sio:SIO_000628
miriam-gene:695
,
lld:C0221026
;
a
sio:SIO_001121
.
}
dgn-np:NP271075.RAJdaPhCu-z6EmnIz__NIyUpoIoPWkfdeO_F2lPR68Ng8130_provenance
{
dgn-np:NP271075.RAJdaPhCu-z6EmnIz__NIyUpoIoPWkfdeO_F2lPR68Ng8130_assertion
dcterms:description
"[These data support the high molecular heterogeneity of BTK gene in XLA disease and provide new insight to the diagnosis and to the role of BTK domain in XLA and in B cell signal transduction and development.]. 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:10612838
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP271075.RAJdaPhCu-z6EmnIz__NIyUpoIoPWkfdeO_F2lPR68Ng8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:48+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
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;
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
"v4.0.0.0" .
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pav:version
"v4.0.0" .
}