@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP674135.RAl17I6seMvqbi1T-q0xua1Lc9PZbHGxjku4ZB6fcnDfk
> .
@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:NP674135.RAl17I6seMvqbi1T-q0xua1Lc9PZbHGxjku4ZB6fcnDfk130_head
{
this:
np:hasAssertion
dgn-np:NP674135.RAl17I6seMvqbi1T-q0xua1Lc9PZbHGxjku4ZB6fcnDfk130_assertion
;
np:hasProvenance
dgn-np:NP674135.RAl17I6seMvqbi1T-q0xua1Lc9PZbHGxjku4ZB6fcnDfk130_provenance
;
np:hasPublicationInfo
dgn-np:NP674135.RAl17I6seMvqbi1T-q0xua1Lc9PZbHGxjku4ZB6fcnDfk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP674135.RAl17I6seMvqbi1T-q0xua1Lc9PZbHGxjku4ZB6fcnDfk130_assertion
a
np:Assertion
.
dgn-np:NP674135.RAl17I6seMvqbi1T-q0xua1Lc9PZbHGxjku4ZB6fcnDfk130_provenance
a
np:Provenance
.
dgn-np:NP674135.RAl17I6seMvqbi1T-q0xua1Lc9PZbHGxjku4ZB6fcnDfk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP674135.RAl17I6seMvqbi1T-q0xua1Lc9PZbHGxjku4ZB6fcnDfk130_assertion
{
miriam-gene:2149
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGNcc6a4a9c1fa41a19307de613751f3ecf
sio:SIO_000628
miriam-gene:2149
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP674135.RAl17I6seMvqbi1T-q0xua1Lc9PZbHGxjku4ZB6fcnDfk130_provenance
{
dgn-np:NP674135.RAl17I6seMvqbi1T-q0xua1Lc9PZbHGxjku4ZB6fcnDfk130_assertion
dcterms:description
"[A rat aortic smooth muscle (RASM) cell cDNA library was screened with a 500-base pair (bp) sequence from the human thrombin receptor, obtained by polymerase chain reaction (PCR) amplification of cDNA synthesized from human erythropoietic leukemia (HEL) cell mRNA with PCR primers based on the published human thrombin receptor sequence.]. 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:1324917
;
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:NP674135.RAl17I6seMvqbi1T-q0xua1Lc9PZbHGxjku4ZB6fcnDfk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:47+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" .
}