Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP229925.RA_uqx8q8zga_MYCm1pF_ZLeQ9s0O7RD0rtQ7mhQjh170130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP229925.RA_uqx8q8zga_MYCm1pF_ZLeQ9s0O7RD0rtQ7mhQjh170130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP229925.RA_uqx8q8zga_MYCm1pF_ZLeQ9s0O7RD0rtQ7mhQjh170130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP229925.RA_uqx8q8zga_MYCm1pF_ZLeQ9s0O7RD0rtQ7mhQjh170130_provenance.
- NP229925.RA_uqx8q8zga_MYCm1pF_ZLeQ9s0O7RD0rtQ7mhQjh170130_assertion description "[A novel mutation (a886g) in exon 5 of FGFR2 in members of a family with Crouzon phenotype and plagiocephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP229925.RA_uqx8q8zga_MYCm1pF_ZLeQ9s0O7RD0rtQ7mhQjh170130_provenance.
- NP229925.RA_uqx8q8zga_MYCm1pF_ZLeQ9s0O7RD0rtQ7mhQjh170130_assertion evidence source_evidence_literature NP229925.RA_uqx8q8zga_MYCm1pF_ZLeQ9s0O7RD0rtQ7mhQjh170130_provenance.
- NP229925.RA_uqx8q8zga_MYCm1pF_ZLeQ9s0O7RD0rtQ7mhQjh170130_assertion SIO_000772 9152842 NP229925.RA_uqx8q8zga_MYCm1pF_ZLeQ9s0O7RD0rtQ7mhQjh170130_provenance.
- NP229925.RA_uqx8q8zga_MYCm1pF_ZLeQ9s0O7RD0rtQ7mhQjh170130_assertion wasDerivedFrom befree-20140225 NP229925.RA_uqx8q8zga_MYCm1pF_ZLeQ9s0O7RD0rtQ7mhQjh170130_provenance.
- NP229925.RA_uqx8q8zga_MYCm1pF_ZLeQ9s0O7RD0rtQ7mhQjh170130_assertion wasGeneratedBy ECO_0000203 NP229925.RA_uqx8q8zga_MYCm1pF_ZLeQ9s0O7RD0rtQ7mhQjh170130_provenance.
- befree-20140225 importedOn "2014-02-25" NP229925.RA_uqx8q8zga_MYCm1pF_ZLeQ9s0O7RD0rtQ7mhQjh170130_provenance.