Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP232325.RAtr-FuflJO1xLhvutvh5doT_Vb5M-4c2N8sdDZorLrug130_assertion> ?p ?o ?g. }
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- NP232325.RAtr-FuflJO1xLhvutvh5doT_Vb5M-4c2N8sdDZorLrug130_assertion type Assertion NP232325.RAtr-FuflJO1xLhvutvh5doT_Vb5M-4c2N8sdDZorLrug130_head.
- NP232325.RAtr-FuflJO1xLhvutvh5doT_Vb5M-4c2N8sdDZorLrug130_assertion description "[Familial isolated primary hyperparathyroidism is a distinct genetic variant of the MEN1 syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP232325.RAtr-FuflJO1xLhvutvh5doT_Vb5M-4c2N8sdDZorLrug130_provenance.
- NP232325.RAtr-FuflJO1xLhvutvh5doT_Vb5M-4c2N8sdDZorLrug130_assertion evidence source_evidence_literature NP232325.RAtr-FuflJO1xLhvutvh5doT_Vb5M-4c2N8sdDZorLrug130_provenance.
- NP232325.RAtr-FuflJO1xLhvutvh5doT_Vb5M-4c2N8sdDZorLrug130_assertion SIO_000772 18084346 NP232325.RAtr-FuflJO1xLhvutvh5doT_Vb5M-4c2N8sdDZorLrug130_provenance.
- NP232325.RAtr-FuflJO1xLhvutvh5doT_Vb5M-4c2N8sdDZorLrug130_assertion wasDerivedFrom lhgdn-20090331 NP232325.RAtr-FuflJO1xLhvutvh5doT_Vb5M-4c2N8sdDZorLrug130_provenance.
- NP232325.RAtr-FuflJO1xLhvutvh5doT_Vb5M-4c2N8sdDZorLrug130_assertion wasGeneratedBy ECO_0000203 NP232325.RAtr-FuflJO1xLhvutvh5doT_Vb5M-4c2N8sdDZorLrug130_provenance.