@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP622164.RAIfvtS1VRxtXtG6rjJTC3mEOZKtuJrdZuTO7ehpEoS-Y
> .
@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:NP622164.RAIfvtS1VRxtXtG6rjJTC3mEOZKtuJrdZuTO7ehpEoS-Y130_head
{
this:
np:hasAssertion
dgn-np:NP622164.RAIfvtS1VRxtXtG6rjJTC3mEOZKtuJrdZuTO7ehpEoS-Y130_assertion
;
np:hasProvenance
dgn-np:NP622164.RAIfvtS1VRxtXtG6rjJTC3mEOZKtuJrdZuTO7ehpEoS-Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP622164.RAIfvtS1VRxtXtG6rjJTC3mEOZKtuJrdZuTO7ehpEoS-Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP622164.RAIfvtS1VRxtXtG6rjJTC3mEOZKtuJrdZuTO7ehpEoS-Y130_assertion
a
np:Assertion
.
dgn-np:NP622164.RAIfvtS1VRxtXtG6rjJTC3mEOZKtuJrdZuTO7ehpEoS-Y130_provenance
a
np:Provenance
.
dgn-np:NP622164.RAIfvtS1VRxtXtG6rjJTC3mEOZKtuJrdZuTO7ehpEoS-Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP622164.RAIfvtS1VRxtXtG6rjJTC3mEOZKtuJrdZuTO7ehpEoS-Y130_assertion
{
miriam-gene:5781
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGN39c61d8b5ff4b7fc85e2b36c1083bc7c
sio:SIO_000628
miriam-gene:5781
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP622164.RAIfvtS1VRxtXtG6rjJTC3mEOZKtuJrdZuTO7ehpEoS-Y130_provenance
{
dgn-np:NP622164.RAIfvtS1VRxtXtG6rjJTC3mEOZKtuJrdZuTO7ehpEoS-Y130_assertion
dcterms:description
"[Our objective was to describe: 1) physicians' knowledge of whether genetic counseling is provided to parents of newborns with sickle cell trait (SCT) or who are cystic fibrosis carriers (CFC), and 2) the prevalence of genetic counseling provided by primary care physicians.]. 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:22903793
;
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:NP622164.RAIfvtS1VRxtXtG6rjJTC3mEOZKtuJrdZuTO7ehpEoS-Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:15+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" .
}