Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP802572.RALUCz48j6FH1tGmRInfaGBD3I7V4iWB_qvlHeYE3EYVk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP802572.RALUCz48j6FH1tGmRInfaGBD3I7V4iWB_qvlHeYE3EYVk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP802572.RALUCz48j6FH1tGmRInfaGBD3I7V4iWB_qvlHeYE3EYVk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP802572.RALUCz48j6FH1tGmRInfaGBD3I7V4iWB_qvlHeYE3EYVk130_provenance.
- NP802572.RALUCz48j6FH1tGmRInfaGBD3I7V4iWB_qvlHeYE3EYVk130_assertion description "[Genetic mutations that disrupt GM-CSF receptor signaling comprise a rare form of hereditary PAP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802572.RALUCz48j6FH1tGmRInfaGBD3I7V4iWB_qvlHeYE3EYVk130_provenance.
- NP802572.RALUCz48j6FH1tGmRInfaGBD3I7V4iWB_qvlHeYE3EYVk130_assertion evidence source_evidence_literature NP802572.RALUCz48j6FH1tGmRInfaGBD3I7V4iWB_qvlHeYE3EYVk130_provenance.
- NP802572.RALUCz48j6FH1tGmRInfaGBD3I7V4iWB_qvlHeYE3EYVk130_assertion SIO_000772 20338813 NP802572.RALUCz48j6FH1tGmRInfaGBD3I7V4iWB_qvlHeYE3EYVk130_provenance.
- NP802572.RALUCz48j6FH1tGmRInfaGBD3I7V4iWB_qvlHeYE3EYVk130_assertion wasDerivedFrom befree-2016 NP802572.RALUCz48j6FH1tGmRInfaGBD3I7V4iWB_qvlHeYE3EYVk130_provenance.
- NP802572.RALUCz48j6FH1tGmRInfaGBD3I7V4iWB_qvlHeYE3EYVk130_assertion wasGeneratedBy ECO_0000203 NP802572.RALUCz48j6FH1tGmRInfaGBD3I7V4iWB_qvlHeYE3EYVk130_provenance.
- befree-2016 importedOn "2016-02-19" NP802572.RALUCz48j6FH1tGmRInfaGBD3I7V4iWB_qvlHeYE3EYVk130_provenance.