Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1231972.RABPqstmL4Fxd9g9_VRzxy_iqEXl3Qu7ekft0V96gBZZI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1231972.RABPqstmL4Fxd9g9_VRzxy_iqEXl3Qu7ekft0V96gBZZI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1231972.RABPqstmL4Fxd9g9_VRzxy_iqEXl3Qu7ekft0V96gBZZI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1231972.RABPqstmL4Fxd9g9_VRzxy_iqEXl3Qu7ekft0V96gBZZI130_provenance.
- NP1231972.RABPqstmL4Fxd9g9_VRzxy_iqEXl3Qu7ekft0V96gBZZI130_assertion description "[Additionally, a literature review allowed us to conclude that KAL1 protein at high levels may interfere with FGFR1 signaling activity, most probably indirectly giving rise to ectrodactyly, intellectual disability, and genital anomalies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1231972.RABPqstmL4Fxd9g9_VRzxy_iqEXl3Qu7ekft0V96gBZZI130_provenance.
- NP1231972.RABPqstmL4Fxd9g9_VRzxy_iqEXl3Qu7ekft0V96gBZZI130_assertion evidence source_evidence_literature NP1231972.RABPqstmL4Fxd9g9_VRzxy_iqEXl3Qu7ekft0V96gBZZI130_provenance.
- NP1231972.RABPqstmL4Fxd9g9_VRzxy_iqEXl3Qu7ekft0V96gBZZI130_assertion SIO_000772 25339597 NP1231972.RABPqstmL4Fxd9g9_VRzxy_iqEXl3Qu7ekft0V96gBZZI130_provenance.
- NP1231972.RABPqstmL4Fxd9g9_VRzxy_iqEXl3Qu7ekft0V96gBZZI130_assertion wasDerivedFrom befree-2016 NP1231972.RABPqstmL4Fxd9g9_VRzxy_iqEXl3Qu7ekft0V96gBZZI130_provenance.
- NP1231972.RABPqstmL4Fxd9g9_VRzxy_iqEXl3Qu7ekft0V96gBZZI130_assertion wasGeneratedBy ECO_0000203 NP1231972.RABPqstmL4Fxd9g9_VRzxy_iqEXl3Qu7ekft0V96gBZZI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1231972.RABPqstmL4Fxd9g9_VRzxy_iqEXl3Qu7ekft0V96gBZZI130_provenance.