Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP948392.RAtuMuhh50Qhb9gs6C4XirV4BA4EIABtYoUQcV3kcMlU4130_assertion> ?p ?o ?g. }
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- NP948392.RAtuMuhh50Qhb9gs6C4XirV4BA4EIABtYoUQcV3kcMlU4130_assertion type Assertion NP948392.RAtuMuhh50Qhb9gs6C4XirV4BA4EIABtYoUQcV3kcMlU4130_head.
- NP948392.RAtuMuhh50Qhb9gs6C4XirV4BA4EIABtYoUQcV3kcMlU4130_assertion description "[SPG11 should be suspected in patients with isolated or recessive HSP, thin corpus callosum and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948392.RAtuMuhh50Qhb9gs6C4XirV4BA4EIABtYoUQcV3kcMlU4130_provenance.
- NP948392.RAtuMuhh50Qhb9gs6C4XirV4BA4EIABtYoUQcV3kcMlU4130_assertion evidence source_evidence_literature NP948392.RAtuMuhh50Qhb9gs6C4XirV4BA4EIABtYoUQcV3kcMlU4130_provenance.
- NP948392.RAtuMuhh50Qhb9gs6C4XirV4BA4EIABtYoUQcV3kcMlU4130_assertion SIO_000772 18439221 NP948392.RAtuMuhh50Qhb9gs6C4XirV4BA4EIABtYoUQcV3kcMlU4130_provenance.
- NP948392.RAtuMuhh50Qhb9gs6C4XirV4BA4EIABtYoUQcV3kcMlU4130_assertion wasDerivedFrom befree-20150227 NP948392.RAtuMuhh50Qhb9gs6C4XirV4BA4EIABtYoUQcV3kcMlU4130_provenance.
- NP948392.RAtuMuhh50Qhb9gs6C4XirV4BA4EIABtYoUQcV3kcMlU4130_assertion wasGeneratedBy ECO_0000203 NP948392.RAtuMuhh50Qhb9gs6C4XirV4BA4EIABtYoUQcV3kcMlU4130_provenance.