@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY
> .
@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:NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY130_head
{
this:
np:hasAssertion
dgn-np:NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY130_assertion
;
np:hasProvenance
dgn-np:NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY130_provenance
;
np:hasPublicationInfo
dgn-np:NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY130_assertion
a
np:Assertion
.
dgn-np:NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY130_provenance
a
np:Provenance
.
dgn-np:NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY130_assertion
{
miriam-gene:3792
a
ncit:C16612
.
lld:C0398568
a
ncit:C7057
.
dgn-gda:DGNe96672c568e0a42c7069b13854b14a8c
sio:SIO_000628
miriam-gene:3792
,
lld:C0398568
;
a
sio:SIO_001121
.
}
dgn-np:NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY130_provenance
{
dgn-np:NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY130_assertion
dcterms:description
"[The latest postulated diagnoses for Henry are the coexistence of both Kell blood group antigenicity (possibly inherited from Jacquetta Woodville, Henry's maternal great grandmother) causing related impaired fertility, and McLeod syndrome, causing psychotic changes.]. 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:24350322
;
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:NP1137942.RAo4b41HbnvcE0A37683auRE16xMnfDVhdfOKHYLmNjcY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:22+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:disgenetv3.0rdf
;
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" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}