Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP687878.RADhGBQHCLVcw--oCVnqF9O1xmo56kQtM1E-BZ1yyd1Cs130_assertion> ?p ?o ?g. }
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- NP687878.RADhGBQHCLVcw--oCVnqF9O1xmo56kQtM1E-BZ1yyd1Cs130_assertion type Assertion NP687878.RADhGBQHCLVcw--oCVnqF9O1xmo56kQtM1E-BZ1yyd1Cs130_head.
- NP687878.RADhGBQHCLVcw--oCVnqF9O1xmo56kQtM1E-BZ1yyd1Cs130_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." NP687878.RADhGBQHCLVcw--oCVnqF9O1xmo56kQtM1E-BZ1yyd1Cs130_provenance.
- NP687878.RADhGBQHCLVcw--oCVnqF9O1xmo56kQtM1E-BZ1yyd1Cs130_assertion evidence source_evidence_literature NP687878.RADhGBQHCLVcw--oCVnqF9O1xmo56kQtM1E-BZ1yyd1Cs130_provenance.
- NP687878.RADhGBQHCLVcw--oCVnqF9O1xmo56kQtM1E-BZ1yyd1Cs130_assertion SIO_000772 12431796 NP687878.RADhGBQHCLVcw--oCVnqF9O1xmo56kQtM1E-BZ1yyd1Cs130_provenance.
- NP687878.RADhGBQHCLVcw--oCVnqF9O1xmo56kQtM1E-BZ1yyd1Cs130_assertion wasDerivedFrom befree-20140225 NP687878.RADhGBQHCLVcw--oCVnqF9O1xmo56kQtM1E-BZ1yyd1Cs130_provenance.
- NP687878.RADhGBQHCLVcw--oCVnqF9O1xmo56kQtM1E-BZ1yyd1Cs130_assertion wasGeneratedBy ECO_0000203 NP687878.RADhGBQHCLVcw--oCVnqF9O1xmo56kQtM1E-BZ1yyd1Cs130_provenance.