Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP374329.RABohR9Lirwe05f9sltiv3Z7-ac_JdMAaVSzN67H9Wz1Y130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP374329.RABohR9Lirwe05f9sltiv3Z7-ac_JdMAaVSzN67H9Wz1Y130_assertion type Assertion NP374329.RABohR9Lirwe05f9sltiv3Z7-ac_JdMAaVSzN67H9Wz1Y130_head.
- NP374329.RABohR9Lirwe05f9sltiv3Z7-ac_JdMAaVSzN67H9Wz1Y130_assertion description "[We tested the hypothesis that a variant of the LIM homeodomain gene LHX4 is responsible for the dwarfism phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374329.RABohR9Lirwe05f9sltiv3Z7-ac_JdMAaVSzN67H9Wz1Y130_provenance.
- NP374329.RABohR9Lirwe05f9sltiv3Z7-ac_JdMAaVSzN67H9Wz1Y130_assertion evidence source_evidence_literature NP374329.RABohR9Lirwe05f9sltiv3Z7-ac_JdMAaVSzN67H9Wz1Y130_provenance.
- NP374329.RABohR9Lirwe05f9sltiv3Z7-ac_JdMAaVSzN67H9Wz1Y130_assertion SIO_000772 12431796 NP374329.RABohR9Lirwe05f9sltiv3Z7-ac_JdMAaVSzN67H9Wz1Y130_provenance.
- NP374329.RABohR9Lirwe05f9sltiv3Z7-ac_JdMAaVSzN67H9Wz1Y130_assertion wasDerivedFrom befree-2016 NP374329.RABohR9Lirwe05f9sltiv3Z7-ac_JdMAaVSzN67H9Wz1Y130_provenance.
- NP374329.RABohR9Lirwe05f9sltiv3Z7-ac_JdMAaVSzN67H9Wz1Y130_assertion wasGeneratedBy ECO_0000203 NP374329.RABohR9Lirwe05f9sltiv3Z7-ac_JdMAaVSzN67H9Wz1Y130_provenance.