Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP152396.RAAwO_L2mVExFo9_cxKNXsYqpzVymQ_dwrO4oTdOAnM4k130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP152396.RAAwO_L2mVExFo9_cxKNXsYqpzVymQ_dwrO4oTdOAnM4k130_assertion type Assertion NP152396.RAAwO_L2mVExFo9_cxKNXsYqpzVymQ_dwrO4oTdOAnM4k130_head.
- NP152396.RAAwO_L2mVExFo9_cxKNXsYqpzVymQ_dwrO4oTdOAnM4k130_assertion wasGeneratedBy ECO_0000203 NP152396.RAAwO_L2mVExFo9_cxKNXsYqpzVymQ_dwrO4oTdOAnM4k130_provenance.
- NP152396.RAAwO_L2mVExFo9_cxKNXsYqpzVymQ_dwrO4oTdOAnM4k130_assertion wasDerivedFrom lhgdn-20090331 NP152396.RAAwO_L2mVExFo9_cxKNXsYqpzVymQ_dwrO4oTdOAnM4k130_provenance.
- NP152396.RAAwO_L2mVExFo9_cxKNXsYqpzVymQ_dwrO4oTdOAnM4k130_assertion SIO_000772 15001591 NP152396.RAAwO_L2mVExFo9_cxKNXsYqpzVymQ_dwrO4oTdOAnM4k130_provenance.
- NP152396.RAAwO_L2mVExFo9_cxKNXsYqpzVymQ_dwrO4oTdOAnM4k130_assertion evidence source_evidence_literature NP152396.RAAwO_L2mVExFo9_cxKNXsYqpzVymQ_dwrO4oTdOAnM4k130_provenance.
- NP152396.RAAwO_L2mVExFo9_cxKNXsYqpzVymQ_dwrO4oTdOAnM4k130_assertion description "[two novel intragenic FGFR1 mutations in two sporadic male cases in Kallmann syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP152396.RAAwO_L2mVExFo9_cxKNXsYqpzVymQ_dwrO4oTdOAnM4k130_provenance.