Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP553150.RAATv-tH_whZbRl8m_559iITneBEqBdjNt4R3IMxrEkOc130_assertion> ?p ?o ?g. }
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- NP553150.RAATv-tH_whZbRl8m_559iITneBEqBdjNt4R3IMxrEkOc130_assertion type Assertion NP553150.RAATv-tH_whZbRl8m_559iITneBEqBdjNt4R3IMxrEkOc130_head.
- NP553150.RAATv-tH_whZbRl8m_559iITneBEqBdjNt4R3IMxrEkOc130_assertion description "[FIHP with primary hyperparathyroidism as the sole endocrinopathy due to a previously unreported heterozygous missense germline MEN1 mutation, Tyr351Asn.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP553150.RAATv-tH_whZbRl8m_559iITneBEqBdjNt4R3IMxrEkOc130_provenance.
- NP553150.RAATv-tH_whZbRl8m_559iITneBEqBdjNt4R3IMxrEkOc130_assertion evidence source_evidence_literature NP553150.RAATv-tH_whZbRl8m_559iITneBEqBdjNt4R3IMxrEkOc130_provenance.
- NP553150.RAATv-tH_whZbRl8m_559iITneBEqBdjNt4R3IMxrEkOc130_assertion SIO_000772 18084346 NP553150.RAATv-tH_whZbRl8m_559iITneBEqBdjNt4R3IMxrEkOc130_provenance.
- NP553150.RAATv-tH_whZbRl8m_559iITneBEqBdjNt4R3IMxrEkOc130_assertion wasDerivedFrom befree-20150227 NP553150.RAATv-tH_whZbRl8m_559iITneBEqBdjNt4R3IMxrEkOc130_provenance.
- NP553150.RAATv-tH_whZbRl8m_559iITneBEqBdjNt4R3IMxrEkOc130_assertion wasGeneratedBy ECO_0000203 NP553150.RAATv-tH_whZbRl8m_559iITneBEqBdjNt4R3IMxrEkOc130_provenance.