Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP152397.RAvZ07P6oWrou74STTVVCydF6XDulMPZRG1-SrtoeA4jY130_assertion> ?p ?o ?g. }
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- NP152397.RAvZ07P6oWrou74STTVVCydF6XDulMPZRG1-SrtoeA4jY130_assertion type Assertion NP152397.RAvZ07P6oWrou74STTVVCydF6XDulMPZRG1-SrtoeA4jY130_head.
- NP152397.RAvZ07P6oWrou74STTVVCydF6XDulMPZRG1-SrtoeA4jY130_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." NP152397.RAvZ07P6oWrou74STTVVCydF6XDulMPZRG1-SrtoeA4jY130_provenance.
- NP152397.RAvZ07P6oWrou74STTVVCydF6XDulMPZRG1-SrtoeA4jY130_assertion evidence source_evidence_literature NP152397.RAvZ07P6oWrou74STTVVCydF6XDulMPZRG1-SrtoeA4jY130_provenance.
- NP152397.RAvZ07P6oWrou74STTVVCydF6XDulMPZRG1-SrtoeA4jY130_assertion SIO_000772 16764984 NP152397.RAvZ07P6oWrou74STTVVCydF6XDulMPZRG1-SrtoeA4jY130_provenance.
- NP152397.RAvZ07P6oWrou74STTVVCydF6XDulMPZRG1-SrtoeA4jY130_assertion wasDerivedFrom lhgdn-20090331 NP152397.RAvZ07P6oWrou74STTVVCydF6XDulMPZRG1-SrtoeA4jY130_provenance.
- NP152397.RAvZ07P6oWrou74STTVVCydF6XDulMPZRG1-SrtoeA4jY130_assertion wasGeneratedBy ECO_0000203 NP152397.RAvZ07P6oWrou74STTVVCydF6XDulMPZRG1-SrtoeA4jY130_provenance.