Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP217688.RAN0AQ0L3a8oGcxQrExv1sh2HXCx-fMmh_6fKB7hnSwkw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP217688.RAN0AQ0L3a8oGcxQrExv1sh2HXCx-fMmh_6fKB7hnSwkw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP217688.RAN0AQ0L3a8oGcxQrExv1sh2HXCx-fMmh_6fKB7hnSwkw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP217688.RAN0AQ0L3a8oGcxQrExv1sh2HXCx-fMmh_6fKB7hnSwkw130_provenance.
- 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.
- lhgdn-20090331 importedOn "2009-03-31" NP217688.RAN0AQ0L3a8oGcxQrExv1sh2HXCx-fMmh_6fKB7hnSwkw130_provenance.