Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP217688.RAN0AQ0L3a8oGcxQrExv1sh2HXCx-fMmh_6fKB7hnSwkw130_assertion> ?p ?o ?g. }
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- NP217688.RAN0AQ0L3a8oGcxQrExv1sh2HXCx-fMmh_6fKB7hnSwkw130_assertion type Assertion NP217688.RAN0AQ0L3a8oGcxQrExv1sh2HXCx-fMmh_6fKB7hnSwkw130_head.
- NP217688.RAN0AQ0L3a8oGcxQrExv1sh2HXCx-fMmh_6fKB7hnSwkw130_assertion description "[Mutations in fibroblast growth factor receptor 1 cause Kallmann syndrome with a wide spectrum of reproductive phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP217688.RAN0AQ0L3a8oGcxQrExv1sh2HXCx-fMmh_6fKB7hnSwkw130_provenance.
- NP217688.RAN0AQ0L3a8oGcxQrExv1sh2HXCx-fMmh_6fKB7hnSwkw130_assertion evidence source_evidence_literature NP217688.RAN0AQ0L3a8oGcxQrExv1sh2HXCx-fMmh_6fKB7hnSwkw130_provenance.
- NP217688.RAN0AQ0L3a8oGcxQrExv1sh2HXCx-fMmh_6fKB7hnSwkw130_assertion SIO_000772 16764984 NP217688.RAN0AQ0L3a8oGcxQrExv1sh2HXCx-fMmh_6fKB7hnSwkw130_provenance.
- NP217688.RAN0AQ0L3a8oGcxQrExv1sh2HXCx-fMmh_6fKB7hnSwkw130_assertion wasDerivedFrom lhgdn-20090331 NP217688.RAN0AQ0L3a8oGcxQrExv1sh2HXCx-fMmh_6fKB7hnSwkw130_provenance.
- NP217688.RAN0AQ0L3a8oGcxQrExv1sh2HXCx-fMmh_6fKB7hnSwkw130_assertion wasGeneratedBy ECO_0000203 NP217688.RAN0AQ0L3a8oGcxQrExv1sh2HXCx-fMmh_6fKB7hnSwkw130_provenance.