Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1393548.RAXi08eULyWlog9Rp3HxvlnccCm2dS76kAXgw8CZaK6vc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1393548.RAXi08eULyWlog9Rp3HxvlnccCm2dS76kAXgw8CZaK6vc130_assertion type Assertion NP1393548.RAXi08eULyWlog9Rp3HxvlnccCm2dS76kAXgw8CZaK6vc130_head.
- NP1393548.RAXi08eULyWlog9Rp3HxvlnccCm2dS76kAXgw8CZaK6vc130_assertion description "[Kallmann syndrome is an inherited disease which is characterised by anosmia (inability to smell) and hypogonadotropic hypogonadism both of which are thought to occur as a result of a failure of correct neuronal migration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1393548.RAXi08eULyWlog9Rp3HxvlnccCm2dS76kAXgw8CZaK6vc130_provenance.
- NP1393548.RAXi08eULyWlog9Rp3HxvlnccCm2dS76kAXgw8CZaK6vc130_assertion evidence source_evidence_literature NP1393548.RAXi08eULyWlog9Rp3HxvlnccCm2dS76kAXgw8CZaK6vc130_provenance.
- NP1393548.RAXi08eULyWlog9Rp3HxvlnccCm2dS76kAXgw8CZaK6vc130_assertion SIO_000772 9554756 NP1393548.RAXi08eULyWlog9Rp3HxvlnccCm2dS76kAXgw8CZaK6vc130_provenance.
- NP1393548.RAXi08eULyWlog9Rp3HxvlnccCm2dS76kAXgw8CZaK6vc130_assertion wasDerivedFrom befree-2016 NP1393548.RAXi08eULyWlog9Rp3HxvlnccCm2dS76kAXgw8CZaK6vc130_provenance.
- NP1393548.RAXi08eULyWlog9Rp3HxvlnccCm2dS76kAXgw8CZaK6vc130_assertion wasGeneratedBy ECO_0000203 NP1393548.RAXi08eULyWlog9Rp3HxvlnccCm2dS76kAXgw8CZaK6vc130_provenance.