@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY
> .
@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:NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY130_head
{
this:
np:hasAssertion
dgn-np:NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY130_assertion
;
np:hasProvenance
dgn-np:NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY130_provenance
;
np:hasPublicationInfo
dgn-np:NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY130_assertion
a
np:Assertion
.
dgn-np:NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY130_provenance
a
np:Provenance
.
dgn-np:NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY130_assertion
{
miriam-gene:1351
a
ncit:C16612
.
lld:C0019069
a
ncit:C7057
.
dgn-gda:DGN63bd43edda926281278601cd829b44a9
sio:SIO_000628
miriam-gene:1351
,
lld:C0019069
;
a
sio:SIO_001121
.
}
dgn-np:NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY130_provenance
{
dgn-np:NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY130_assertion
dcterms:description
"[The identification of fetal genetic disease has, for the most part, relied on examination of an end product, such as analysis of factor VIII levels obtained from cord blood in fetuses at risk for hemophilia.]. 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:7858372
;
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:NP1324036.RAQI0oXfmgAU_KipDuq0iVEuGhH5cXgCHFHCwSaPvOucY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:46+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" .
}