@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP870153.RAhWLm-nhFmZw9aIc2OkH-AI7pzbqEF46g3vPNSMy1gtc130_head { this: np:hasAssertion dgn-np:NP870153.RAhWLm-nhFmZw9aIc2OkH-AI7pzbqEF46g3vPNSMy1gtc130_assertion; np:hasProvenance dgn-np:NP870153.RAhWLm-nhFmZw9aIc2OkH-AI7pzbqEF46g3vPNSMy1gtc130_provenance; np:hasPublicationInfo dgn-np:NP870153.RAhWLm-nhFmZw9aIc2OkH-AI7pzbqEF46g3vPNSMy1gtc130_publicationInfo; a np:Nanopublication . dgn-np:NP870153.RAhWLm-nhFmZw9aIc2OkH-AI7pzbqEF46g3vPNSMy1gtc130_assertion a np:Assertion . dgn-np:NP870153.RAhWLm-nhFmZw9aIc2OkH-AI7pzbqEF46g3vPNSMy1gtc130_provenance a np:Provenance . dgn-np:NP870153.RAhWLm-nhFmZw9aIc2OkH-AI7pzbqEF46g3vPNSMy1gtc130_publicationInfo a np:PublicationInfo . } dgn-np:NP870153.RAhWLm-nhFmZw9aIc2OkH-AI7pzbqEF46g3vPNSMy1gtc130_assertion { miriam-gene:11151 a ncit:C16612 . lld:C0020217 a ncit:C7057 . dgn-gda:DGNf1fc53f687bfd4d9154438f13d6903a1 sio:SIO_000628 miriam-gene:11151, lld:C0020217; a sio:SIO_001121 . } dgn-np:NP870153.RAhWLm-nhFmZw9aIc2OkH-AI7pzbqEF46g3vPNSMy1gtc130_provenance { dgn-np:NP870153.RAhWLm-nhFmZw9aIc2OkH-AI7pzbqEF46g3vPNSMy1gtc130_assertion dcterms:description "[The unique genetic features of CHMs (androgenetic diploidy), PHMs (diandric triploidy), and nonmolar specimens (biparental diploidy) allow for certain molecular techniques, including immunohistochemical analysis of p57 expression (a paternally imprinted maternally expressed gene) and molecular genotyping, to refine the diagnosis of hydatidiform moles.]. 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:21293291; 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:NP870153.RAhWLm-nhFmZw9aIc2OkH-AI7pzbqEF46g3vPNSMy1gtc130_publicationInfo { this: dcterms:created "2016-05-13T12:48:19+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }