Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1211442.RAkpmvahDU38awq-moB-qfigVjDKZPtKX4l2WS4S03rf4130_assertion> ?p ?o ?g. }
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- NP1211442.RAkpmvahDU38awq-moB-qfigVjDKZPtKX4l2WS4S03rf4130_assertion type Assertion NP1211442.RAkpmvahDU38awq-moB-qfigVjDKZPtKX4l2WS4S03rf4130_head.
- NP1211442.RAkpmvahDU38awq-moB-qfigVjDKZPtKX4l2WS4S03rf4130_assertion description "[Both our patients had additional bilateral cryptorchidism, a key phenotypic feature in males with FGF8 associated Kallmann syndrome.Each mutation was paternally inherited.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1211442.RAkpmvahDU38awq-moB-qfigVjDKZPtKX4l2WS4S03rf4130_provenance.
- NP1211442.RAkpmvahDU38awq-moB-qfigVjDKZPtKX4l2WS4S03rf4130_assertion evidence source_evidence_literature NP1211442.RAkpmvahDU38awq-moB-qfigVjDKZPtKX4l2WS4S03rf4130_provenance.
- NP1211442.RAkpmvahDU38awq-moB-qfigVjDKZPtKX4l2WS4S03rf4130_assertion SIO_000772 25131394 NP1211442.RAkpmvahDU38awq-moB-qfigVjDKZPtKX4l2WS4S03rf4130_provenance.
- NP1211442.RAkpmvahDU38awq-moB-qfigVjDKZPtKX4l2WS4S03rf4130_assertion wasDerivedFrom befree-2016 NP1211442.RAkpmvahDU38awq-moB-qfigVjDKZPtKX4l2WS4S03rf4130_provenance.
- NP1211442.RAkpmvahDU38awq-moB-qfigVjDKZPtKX4l2WS4S03rf4130_assertion wasGeneratedBy ECO_0000203 NP1211442.RAkpmvahDU38awq-moB-qfigVjDKZPtKX4l2WS4S03rf4130_provenance.