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- source_evidence_literature type ECO_0000212 NP374329.RABohR9Lirwe05f9sltiv3Z7-ac_JdMAaVSzN67H9Wz1Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP374329.RABohR9Lirwe05f9sltiv3Z7-ac_JdMAaVSzN67H9Wz1Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP374329.RABohR9Lirwe05f9sltiv3Z7-ac_JdMAaVSzN67H9Wz1Y130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP374329.RABohR9Lirwe05f9sltiv3Z7-ac_JdMAaVSzN67H9Wz1Y130_provenance.