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- source_evidence_literature type ECO_0000212 NP874167.RAfKAzAZk_Q0FvxlUg2tnMgeqNO4KJ_kWjW1WTR7GRn2U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP874167.RAfKAzAZk_Q0FvxlUg2tnMgeqNO4KJ_kWjW1WTR7GRn2U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP874167.RAfKAzAZk_Q0FvxlUg2tnMgeqNO4KJ_kWjW1WTR7GRn2U130_provenance.
- NP874167.RAfKAzAZk_Q0FvxlUg2tnMgeqNO4KJ_kWjW1WTR7GRn2U130_assertion description "[Co-occurring PTPN11 and SOS1 gene mutations in Noonan syndrome: does this predict a more severe phenotype?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP874167.RAfKAzAZk_Q0FvxlUg2tnMgeqNO4KJ_kWjW1WTR7GRn2U130_provenance.
- NP874167.RAfKAzAZk_Q0FvxlUg2tnMgeqNO4KJ_kWjW1WTR7GRn2U130_assertion evidence source_evidence_literature NP874167.RAfKAzAZk_Q0FvxlUg2tnMgeqNO4KJ_kWjW1WTR7GRn2U130_provenance.
- NP874167.RAfKAzAZk_Q0FvxlUg2tnMgeqNO4KJ_kWjW1WTR7GRn2U130_assertion SIO_000772 21340158 NP874167.RAfKAzAZk_Q0FvxlUg2tnMgeqNO4KJ_kWjW1WTR7GRn2U130_provenance.
- NP874167.RAfKAzAZk_Q0FvxlUg2tnMgeqNO4KJ_kWjW1WTR7GRn2U130_assertion wasDerivedFrom befree-2016 NP874167.RAfKAzAZk_Q0FvxlUg2tnMgeqNO4KJ_kWjW1WTR7GRn2U130_provenance.
- NP874167.RAfKAzAZk_Q0FvxlUg2tnMgeqNO4KJ_kWjW1WTR7GRn2U130_assertion wasGeneratedBy ECO_0000203 NP874167.RAfKAzAZk_Q0FvxlUg2tnMgeqNO4KJ_kWjW1WTR7GRn2U130_provenance.
- befree-2016 importedOn "2016-02-19" NP874167.RAfKAzAZk_Q0FvxlUg2tnMgeqNO4KJ_kWjW1WTR7GRn2U130_provenance.