Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP781648.RAd7jdEc9jkGXNM6pMQJIfzM68YzDL2GWWw1qeEP2TrkE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP781648.RAd7jdEc9jkGXNM6pMQJIfzM68YzDL2GWWw1qeEP2TrkE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP781648.RAd7jdEc9jkGXNM6pMQJIfzM68YzDL2GWWw1qeEP2TrkE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP781648.RAd7jdEc9jkGXNM6pMQJIfzM68YzDL2GWWw1qeEP2TrkE130_provenance.
- NP781648.RAd7jdEc9jkGXNM6pMQJIfzM68YzDL2GWWw1qeEP2TrkE130_assertion description "[Three individuals with smaller, nonrecurrent deletions (?180-500 kb) that include HIP1 but not YWHAG suggest that deletion of HIP1 is sufficient to cause neurological disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP781648.RAd7jdEc9jkGXNM6pMQJIfzM68YzDL2GWWw1qeEP2TrkE130_provenance.
- NP781648.RAd7jdEc9jkGXNM6pMQJIfzM68YzDL2GWWw1qeEP2TrkE130_assertion evidence source_evidence_literature NP781648.RAd7jdEc9jkGXNM6pMQJIfzM68YzDL2GWWw1qeEP2TrkE130_provenance.
- NP781648.RAd7jdEc9jkGXNM6pMQJIfzM68YzDL2GWWw1qeEP2TrkE130_assertion SIO_000772 21109226 NP781648.RAd7jdEc9jkGXNM6pMQJIfzM68YzDL2GWWw1qeEP2TrkE130_provenance.
- NP781648.RAd7jdEc9jkGXNM6pMQJIfzM68YzDL2GWWw1qeEP2TrkE130_assertion wasDerivedFrom befree-20150227 NP781648.RAd7jdEc9jkGXNM6pMQJIfzM68YzDL2GWWw1qeEP2TrkE130_provenance.
- NP781648.RAd7jdEc9jkGXNM6pMQJIfzM68YzDL2GWWw1qeEP2TrkE130_assertion wasGeneratedBy ECO_0000203 NP781648.RAd7jdEc9jkGXNM6pMQJIfzM68YzDL2GWWw1qeEP2TrkE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP781648.RAd7jdEc9jkGXNM6pMQJIfzM68YzDL2GWWw1qeEP2TrkE130_provenance.