Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP536308.RAm1vEtlq0808cDdcihy-JGGTrhCgtiqZeb2opA9VoJg8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP536308.RAm1vEtlq0808cDdcihy-JGGTrhCgtiqZeb2opA9VoJg8130_assertion type Assertion NP536308.RAm1vEtlq0808cDdcihy-JGGTrhCgtiqZeb2opA9VoJg8130_head.
- NP536308.RAm1vEtlq0808cDdcihy-JGGTrhCgtiqZeb2opA9VoJg8130_assertion wasGeneratedBy ECO_0000203 NP536308.RAm1vEtlq0808cDdcihy-JGGTrhCgtiqZeb2opA9VoJg8130_provenance.
- NP536308.RAm1vEtlq0808cDdcihy-JGGTrhCgtiqZeb2opA9VoJg8130_assertion wasDerivedFrom befree-20150227 NP536308.RAm1vEtlq0808cDdcihy-JGGTrhCgtiqZeb2opA9VoJg8130_provenance.
- NP536308.RAm1vEtlq0808cDdcihy-JGGTrhCgtiqZeb2opA9VoJg8130_assertion SIO_000772 19551906 NP536308.RAm1vEtlq0808cDdcihy-JGGTrhCgtiqZeb2opA9VoJg8130_provenance.
- NP536308.RAm1vEtlq0808cDdcihy-JGGTrhCgtiqZeb2opA9VoJg8130_assertion evidence source_evidence_literature NP536308.RAm1vEtlq0808cDdcihy-JGGTrhCgtiqZeb2opA9VoJg8130_provenance.
- NP536308.RAm1vEtlq0808cDdcihy-JGGTrhCgtiqZeb2opA9VoJg8130_assertion description "[Leydig cell hypoplasia (LCH) is a rare form of male pseudohermaphroditism caused by inactivating mutations in the luteinizing hormone receptor gene (LHCGR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP536308.RAm1vEtlq0808cDdcihy-JGGTrhCgtiqZeb2opA9VoJg8130_provenance.