@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP402289.RAochBFUfdXgfGMeMeGS1sJFWbZAMsCYyppsgbe9U8zmc
> .
@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:NP402289.RAochBFUfdXgfGMeMeGS1sJFWbZAMsCYyppsgbe9U8zmc130_head
{
this:
np:hasAssertion
dgn-np:NP402289.RAochBFUfdXgfGMeMeGS1sJFWbZAMsCYyppsgbe9U8zmc130_assertion
;
np:hasProvenance
dgn-np:NP402289.RAochBFUfdXgfGMeMeGS1sJFWbZAMsCYyppsgbe9U8zmc130_provenance
;
np:hasPublicationInfo
dgn-np:NP402289.RAochBFUfdXgfGMeMeGS1sJFWbZAMsCYyppsgbe9U8zmc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP402289.RAochBFUfdXgfGMeMeGS1sJFWbZAMsCYyppsgbe9U8zmc130_assertion
a
np:Assertion
.
dgn-np:NP402289.RAochBFUfdXgfGMeMeGS1sJFWbZAMsCYyppsgbe9U8zmc130_provenance
a
np:Provenance
.
dgn-np:NP402289.RAochBFUfdXgfGMeMeGS1sJFWbZAMsCYyppsgbe9U8zmc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP402289.RAochBFUfdXgfGMeMeGS1sJFWbZAMsCYyppsgbe9U8zmc130_assertion
{
miriam-gene:174
a
ncit:C16612
.
lld:C0039538
a
ncit:C7057
.
dgn-gda:DGNa06bd262d7deec79d271e713d7ccd579
sio:SIO_000628
miriam-gene:174
,
lld:C0039538
;
a
sio:SIO_001121
.
}
dgn-np:NP402289.RAochBFUfdXgfGMeMeGS1sJFWbZAMsCYyppsgbe9U8zmc130_provenance
{
dgn-np:NP402289.RAochBFUfdXgfGMeMeGS1sJFWbZAMsCYyppsgbe9U8zmc130_assertion
dcterms:description
"[In vivo, hESCs lacking EpCAM were able to form teratomas containing tissues representing the three germ layers, and gene expression analysis yielded marked increase in the endoderm marker alpha fetoprotein compared with control.]. 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:19785009
;
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:NP402289.RAochBFUfdXgfGMeMeGS1sJFWbZAMsCYyppsgbe9U8zmc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:59+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" .
}