Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP237263.RA44m8kFEDGRGq7rmL4XqKYlPx83CKfM_smHfkRPzgCvw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP237263.RA44m8kFEDGRGq7rmL4XqKYlPx83CKfM_smHfkRPzgCvw130_assertion type Assertion NP237263.RA44m8kFEDGRGq7rmL4XqKYlPx83CKfM_smHfkRPzgCvw130_head.
- NP237263.RA44m8kFEDGRGq7rmL4XqKYlPx83CKfM_smHfkRPzgCvw130_assertion description "[three new exonic LHX4 allelic variants with at least one being responsible for congenital hypopituitarism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP237263.RA44m8kFEDGRGq7rmL4XqKYlPx83CKfM_smHfkRPzgCvw130_provenance.
- NP237263.RA44m8kFEDGRGq7rmL4XqKYlPx83CKfM_smHfkRPzgCvw130_assertion evidence source_evidence_literature NP237263.RA44m8kFEDGRGq7rmL4XqKYlPx83CKfM_smHfkRPzgCvw130_provenance.
- NP237263.RA44m8kFEDGRGq7rmL4XqKYlPx83CKfM_smHfkRPzgCvw130_assertion SIO_000772 18445675 NP237263.RA44m8kFEDGRGq7rmL4XqKYlPx83CKfM_smHfkRPzgCvw130_provenance.
- NP237263.RA44m8kFEDGRGq7rmL4XqKYlPx83CKfM_smHfkRPzgCvw130_assertion wasDerivedFrom lhgdn-20090331 NP237263.RA44m8kFEDGRGq7rmL4XqKYlPx83CKfM_smHfkRPzgCvw130_provenance.
- NP237263.RA44m8kFEDGRGq7rmL4XqKYlPx83CKfM_smHfkRPzgCvw130_assertion wasGeneratedBy ECO_0000203 NP237263.RA44m8kFEDGRGq7rmL4XqKYlPx83CKfM_smHfkRPzgCvw130_provenance.