Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1175563.RAh_qaTvxTbiTSV622_0-GthEA6CUKge8I1xNPxltWFK0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1175563.RAh_qaTvxTbiTSV622_0-GthEA6CUKge8I1xNPxltWFK0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1175563.RAh_qaTvxTbiTSV622_0-GthEA6CUKge8I1xNPxltWFK0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1175563.RAh_qaTvxTbiTSV622_0-GthEA6CUKge8I1xNPxltWFK0130_provenance.
- NP1175563.RAh_qaTvxTbiTSV622_0-GthEA6CUKge8I1xNPxltWFK0130_assertion description "[Array-CGH analysis of the patient blood revealed a constitutive 1.4 million base pair deletion at 7q11.23, compatible with WS diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1175563.RAh_qaTvxTbiTSV622_0-GthEA6CUKge8I1xNPxltWFK0130_provenance.
- NP1175563.RAh_qaTvxTbiTSV622_0-GthEA6CUKge8I1xNPxltWFK0130_assertion evidence source_evidence_literature NP1175563.RAh_qaTvxTbiTSV622_0-GthEA6CUKge8I1xNPxltWFK0130_provenance.
- NP1175563.RAh_qaTvxTbiTSV622_0-GthEA6CUKge8I1xNPxltWFK0130_assertion SIO_000772 24753445 NP1175563.RAh_qaTvxTbiTSV622_0-GthEA6CUKge8I1xNPxltWFK0130_provenance.
- NP1175563.RAh_qaTvxTbiTSV622_0-GthEA6CUKge8I1xNPxltWFK0130_assertion wasDerivedFrom befree-2016 NP1175563.RAh_qaTvxTbiTSV622_0-GthEA6CUKge8I1xNPxltWFK0130_provenance.
- NP1175563.RAh_qaTvxTbiTSV622_0-GthEA6CUKge8I1xNPxltWFK0130_assertion wasGeneratedBy ECO_0000203 NP1175563.RAh_qaTvxTbiTSV622_0-GthEA6CUKge8I1xNPxltWFK0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1175563.RAh_qaTvxTbiTSV622_0-GthEA6CUKge8I1xNPxltWFK0130_provenance.