Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP650645.RAjgQbBwTzp9uMOEbagb1Z99uFJer8dZVLd5SR5cB68R8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP650645.RAjgQbBwTzp9uMOEbagb1Z99uFJer8dZVLd5SR5cB68R8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP650645.RAjgQbBwTzp9uMOEbagb1Z99uFJer8dZVLd5SR5cB68R8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP650645.RAjgQbBwTzp9uMOEbagb1Z99uFJer8dZVLd5SR5cB68R8130_provenance.
- NP650645.RAjgQbBwTzp9uMOEbagb1Z99uFJer8dZVLd5SR5cB68R8130_assertion description "[Comparison of the phenotypic features in a total of 19 patients with del(17)(p11.2p11.2) shows a consistent clinical phenotype with moderate to severe mental retardation, microbrachycelphaly, prominent forehead, broad face, flat midface, prognathism, short, broad hands, and behavioural anomalies such as self-mutilation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650645.RAjgQbBwTzp9uMOEbagb1Z99uFJer8dZVLd5SR5cB68R8130_provenance.
- NP650645.RAjgQbBwTzp9uMOEbagb1Z99uFJer8dZVLd5SR5cB68R8130_assertion evidence source_evidence_literature NP650645.RAjgQbBwTzp9uMOEbagb1Z99uFJer8dZVLd5SR5cB68R8130_provenance.
- NP650645.RAjgQbBwTzp9uMOEbagb1Z99uFJer8dZVLd5SR5cB68R8130_assertion SIO_000772 3236351 NP650645.RAjgQbBwTzp9uMOEbagb1Z99uFJer8dZVLd5SR5cB68R8130_provenance.
- NP650645.RAjgQbBwTzp9uMOEbagb1Z99uFJer8dZVLd5SR5cB68R8130_assertion wasDerivedFrom befree-20140225 NP650645.RAjgQbBwTzp9uMOEbagb1Z99uFJer8dZVLd5SR5cB68R8130_provenance.
- NP650645.RAjgQbBwTzp9uMOEbagb1Z99uFJer8dZVLd5SR5cB68R8130_assertion wasGeneratedBy ECO_0000203 NP650645.RAjgQbBwTzp9uMOEbagb1Z99uFJer8dZVLd5SR5cB68R8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP650645.RAjgQbBwTzp9uMOEbagb1Z99uFJer8dZVLd5SR5cB68R8130_provenance.