Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP14800.RAVYXR6dXGanAV5-8erGac22gcqCE--xKW7md_48I0c6k130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP14800.RAVYXR6dXGanAV5-8erGac22gcqCE--xKW7md_48I0c6k130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP14800.RAVYXR6dXGanAV5-8erGac22gcqCE--xKW7md_48I0c6k130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP14800.RAVYXR6dXGanAV5-8erGac22gcqCE--xKW7md_48I0c6k130_provenance.
- NP14800.RAVYXR6dXGanAV5-8erGac22gcqCE--xKW7md_48I0c6k130_assertion description "[Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP14800.RAVYXR6dXGanAV5-8erGac22gcqCE--xKW7md_48I0c6k130_provenance.
- NP14800.RAVYXR6dXGanAV5-8erGac22gcqCE--xKW7md_48I0c6k130_assertion evidence source_evidence_curated NP14800.RAVYXR6dXGanAV5-8erGac22gcqCE--xKW7md_48I0c6k130_provenance.
- NP14800.RAVYXR6dXGanAV5-8erGac22gcqCE--xKW7md_48I0c6k130_assertion SIO_000772 19855393 NP14800.RAVYXR6dXGanAV5-8erGac22gcqCE--xKW7md_48I0c6k130_provenance.
- NP14800.RAVYXR6dXGanAV5-8erGac22gcqCE--xKW7md_48I0c6k130_assertion wasDerivedFrom ctd_human-20150221 NP14800.RAVYXR6dXGanAV5-8erGac22gcqCE--xKW7md_48I0c6k130_provenance.
- NP14800.RAVYXR6dXGanAV5-8erGac22gcqCE--xKW7md_48I0c6k130_assertion wasGeneratedBy ECO_0000218 NP14800.RAVYXR6dXGanAV5-8erGac22gcqCE--xKW7md_48I0c6k130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP14800.RAVYXR6dXGanAV5-8erGac22gcqCE--xKW7md_48I0c6k130_provenance.