Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP203889.RANRSD9FzvPwMjB-z2K3msfq2cZWYXygW8YyC3XP-2Gio130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP203889.RANRSD9FzvPwMjB-z2K3msfq2cZWYXygW8YyC3XP-2Gio130_assertion type Assertion NP203889.RANRSD9FzvPwMjB-z2K3msfq2cZWYXygW8YyC3XP-2Gio130_head.
- NP203889.RANRSD9FzvPwMjB-z2K3msfq2cZWYXygW8YyC3XP-2Gio130_assertion wasGeneratedBy ECO_0000203 NP203889.RANRSD9FzvPwMjB-z2K3msfq2cZWYXygW8YyC3XP-2Gio130_provenance.
- NP203889.RANRSD9FzvPwMjB-z2K3msfq2cZWYXygW8YyC3XP-2Gio130_assertion wasDerivedFrom lhgdn-20090331 NP203889.RANRSD9FzvPwMjB-z2K3msfq2cZWYXygW8YyC3XP-2Gio130_provenance.
- NP203889.RANRSD9FzvPwMjB-z2K3msfq2cZWYXygW8YyC3XP-2Gio130_assertion SIO_000772 15001591 NP203889.RANRSD9FzvPwMjB-z2K3msfq2cZWYXygW8YyC3XP-2Gio130_provenance.
- NP203889.RANRSD9FzvPwMjB-z2K3msfq2cZWYXygW8YyC3XP-2Gio130_assertion evidence source_evidence_literature NP203889.RANRSD9FzvPwMjB-z2K3msfq2cZWYXygW8YyC3XP-2Gio130_provenance.
- NP203889.RANRSD9FzvPwMjB-z2K3msfq2cZWYXygW8YyC3XP-2Gio130_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." NP203889.RANRSD9FzvPwMjB-z2K3msfq2cZWYXygW8YyC3XP-2Gio130_provenance.