Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_assertion type Assertion NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_head.
- NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_assertion description "[In addition, another unreported heterozygous missense germline MEN1 mutation, Trp220Leu, was identified in an unrelated male patient with FIHP, whose mother and sister also had primary hyperparathyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_provenance.
- NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_assertion evidence source_evidence_literature NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_provenance.
- NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_assertion SIO_000772 18084346 NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_provenance.
- NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_assertion wasDerivedFrom befree-2016 NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_provenance.
- NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_assertion wasGeneratedBy ECO_0000203 NP645572.RASHmmkq4L8URPW9714r_ADq2VptSJmkCHhB0tAaFiEIs130_provenance.