Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP237263.RA44m8kFEDGRGq7rmL4XqKYlPx83CKfM_smHfkRPzgCvw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP237263.RA44m8kFEDGRGq7rmL4XqKYlPx83CKfM_smHfkRPzgCvw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP237263.RA44m8kFEDGRGq7rmL4XqKYlPx83CKfM_smHfkRPzgCvw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP237263.RA44m8kFEDGRGq7rmL4XqKYlPx83CKfM_smHfkRPzgCvw130_provenance.
- 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.
- lhgdn-20090331 importedOn "2009-03-31" NP237263.RA44m8kFEDGRGq7rmL4XqKYlPx83CKfM_smHfkRPzgCvw130_provenance.