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- source_evidence_literature type ECO_0000212 NP914253.RAawLgcn3OQsy-f7OfdwPjkebcrpSCPJuSGjDdPr6j_fk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914253.RAawLgcn3OQsy-f7OfdwPjkebcrpSCPJuSGjDdPr6j_fk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914253.RAawLgcn3OQsy-f7OfdwPjkebcrpSCPJuSGjDdPr6j_fk130_provenance.
- NP914253.RAawLgcn3OQsy-f7OfdwPjkebcrpSCPJuSGjDdPr6j_fk130_assertion description "[PITX2 mutations are known to be responsible for Axenfield Rieger syndrome, a genetic disorder in which pituitary abnormalities have been detected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914253.RAawLgcn3OQsy-f7OfdwPjkebcrpSCPJuSGjDdPr6j_fk130_provenance.
- NP914253.RAawLgcn3OQsy-f7OfdwPjkebcrpSCPJuSGjDdPr6j_fk130_assertion evidence source_evidence_literature NP914253.RAawLgcn3OQsy-f7OfdwPjkebcrpSCPJuSGjDdPr6j_fk130_provenance.
- NP914253.RAawLgcn3OQsy-f7OfdwPjkebcrpSCPJuSGjDdPr6j_fk130_assertion SIO_000772 21810944 NP914253.RAawLgcn3OQsy-f7OfdwPjkebcrpSCPJuSGjDdPr6j_fk130_provenance.
- NP914253.RAawLgcn3OQsy-f7OfdwPjkebcrpSCPJuSGjDdPr6j_fk130_assertion wasDerivedFrom befree-2016 NP914253.RAawLgcn3OQsy-f7OfdwPjkebcrpSCPJuSGjDdPr6j_fk130_provenance.
- NP914253.RAawLgcn3OQsy-f7OfdwPjkebcrpSCPJuSGjDdPr6j_fk130_assertion wasGeneratedBy ECO_0000203 NP914253.RAawLgcn3OQsy-f7OfdwPjkebcrpSCPJuSGjDdPr6j_fk130_provenance.
- befree-2016 importedOn "2016-02-19" NP914253.RAawLgcn3OQsy-f7OfdwPjkebcrpSCPJuSGjDdPr6j_fk130_provenance.