@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP393448.RAAIxVs751e4XXm2FFl2Vxbj3vfMz0yoVL1FBFWTJWPJ0
> .
@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:NP393448.RAAIxVs751e4XXm2FFl2Vxbj3vfMz0yoVL1FBFWTJWPJ0130_head
{
this:
np:hasAssertion
dgn-np:NP393448.RAAIxVs751e4XXm2FFl2Vxbj3vfMz0yoVL1FBFWTJWPJ0130_assertion
;
np:hasProvenance
dgn-np:NP393448.RAAIxVs751e4XXm2FFl2Vxbj3vfMz0yoVL1FBFWTJWPJ0130_provenance
;
np:hasPublicationInfo
dgn-np:NP393448.RAAIxVs751e4XXm2FFl2Vxbj3vfMz0yoVL1FBFWTJWPJ0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP393448.RAAIxVs751e4XXm2FFl2Vxbj3vfMz0yoVL1FBFWTJWPJ0130_assertion
a
np:Assertion
.
dgn-np:NP393448.RAAIxVs751e4XXm2FFl2Vxbj3vfMz0yoVL1FBFWTJWPJ0130_provenance
a
np:Provenance
.
dgn-np:NP393448.RAAIxVs751e4XXm2FFl2Vxbj3vfMz0yoVL1FBFWTJWPJ0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP393448.RAAIxVs751e4XXm2FFl2Vxbj3vfMz0yoVL1FBFWTJWPJ0130_assertion
{
miriam-gene:174
a
ncit:C16612
.
lld:C0041107
a
ncit:C7057
.
dgn-gda:DGN199c587a586aee0e8342af2fc5b5a1ef
sio:SIO_000628
miriam-gene:174
,
lld:C0041107
;
a
sio:SIO_001121
.
}
dgn-np:NP393448.RAAIxVs751e4XXm2FFl2Vxbj3vfMz0yoVL1FBFWTJWPJ0130_provenance
{
dgn-np:NP393448.RAAIxVs751e4XXm2FFl2Vxbj3vfMz0yoVL1FBFWTJWPJ0130_assertion
dcterms:description
"[Since placental trisomy 16 as well as cases with increased alpha-fetoprotein (AFP) and human chorionic gonadotropin (hCG) are associated with (intrauterine growth retardation (IUGR), oligohydramnios, and fetal demise, at least some cases with this atypical biochemical profile could be explained by this chromosomal abnormality.]. 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:8750291
;
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:NP393448.RAAIxVs751e4XXm2FFl2Vxbj3vfMz0yoVL1FBFWTJWPJ0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:54+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" .
}