Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1034859.RAyV21qS5C6n4oW5U3aS7KTehDucrpbwtMS9k9wFm_Klw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1034859.RAyV21qS5C6n4oW5U3aS7KTehDucrpbwtMS9k9wFm_Klw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1034859.RAyV21qS5C6n4oW5U3aS7KTehDucrpbwtMS9k9wFm_Klw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1034859.RAyV21qS5C6n4oW5U3aS7KTehDucrpbwtMS9k9wFm_Klw130_provenance.
- NP1034859.RAyV21qS5C6n4oW5U3aS7KTehDucrpbwtMS9k9wFm_Klw130_assertion description "[FATP4 mutations in humans cause ichthyosis prematurity syndrome (IPS), and mutations of Fatp4 in mice have previously been found to cause a phenotype that resembles human congenital ichthyoses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1034859.RAyV21qS5C6n4oW5U3aS7KTehDucrpbwtMS9k9wFm_Klw130_provenance.
- NP1034859.RAyV21qS5C6n4oW5U3aS7KTehDucrpbwtMS9k9wFm_Klw130_assertion evidence source_evidence_literature NP1034859.RAyV21qS5C6n4oW5U3aS7KTehDucrpbwtMS9k9wFm_Klw130_provenance.
- NP1034859.RAyV21qS5C6n4oW5U3aS7KTehDucrpbwtMS9k9wFm_Klw130_assertion SIO_000772 23226340 NP1034859.RAyV21qS5C6n4oW5U3aS7KTehDucrpbwtMS9k9wFm_Klw130_provenance.
- NP1034859.RAyV21qS5C6n4oW5U3aS7KTehDucrpbwtMS9k9wFm_Klw130_assertion wasDerivedFrom befree-2016 NP1034859.RAyV21qS5C6n4oW5U3aS7KTehDucrpbwtMS9k9wFm_Klw130_provenance.
- NP1034859.RAyV21qS5C6n4oW5U3aS7KTehDucrpbwtMS9k9wFm_Klw130_assertion wasGeneratedBy ECO_0000203 NP1034859.RAyV21qS5C6n4oW5U3aS7KTehDucrpbwtMS9k9wFm_Klw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1034859.RAyV21qS5C6n4oW5U3aS7KTehDucrpbwtMS9k9wFm_Klw130_provenance.