Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP400482.RAdMmQarpK0b-ZTg-K_Vu4_XOVIfgemeqni10Z_BOdA2U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP400482.RAdMmQarpK0b-ZTg-K_Vu4_XOVIfgemeqni10Z_BOdA2U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP400482.RAdMmQarpK0b-ZTg-K_Vu4_XOVIfgemeqni10Z_BOdA2U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP400482.RAdMmQarpK0b-ZTg-K_Vu4_XOVIfgemeqni10Z_BOdA2U130_provenance.
- NP400482.RAdMmQarpK0b-ZTg-K_Vu4_XOVIfgemeqni10Z_BOdA2U130_assertion description "[FGFR1 and FGFR2 mutations in Pfeiffer syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400482.RAdMmQarpK0b-ZTg-K_Vu4_XOVIfgemeqni10Z_BOdA2U130_provenance.
- NP400482.RAdMmQarpK0b-ZTg-K_Vu4_XOVIfgemeqni10Z_BOdA2U130_assertion evidence source_evidence_literature NP400482.RAdMmQarpK0b-ZTg-K_Vu4_XOVIfgemeqni10Z_BOdA2U130_provenance.
- NP400482.RAdMmQarpK0b-ZTg-K_Vu4_XOVIfgemeqni10Z_BOdA2U130_assertion SIO_000772 23348274 NP400482.RAdMmQarpK0b-ZTg-K_Vu4_XOVIfgemeqni10Z_BOdA2U130_provenance.
- NP400482.RAdMmQarpK0b-ZTg-K_Vu4_XOVIfgemeqni10Z_BOdA2U130_assertion wasDerivedFrom befree-20150227 NP400482.RAdMmQarpK0b-ZTg-K_Vu4_XOVIfgemeqni10Z_BOdA2U130_provenance.
- NP400482.RAdMmQarpK0b-ZTg-K_Vu4_XOVIfgemeqni10Z_BOdA2U130_assertion wasGeneratedBy ECO_0000203 NP400482.RAdMmQarpK0b-ZTg-K_Vu4_XOVIfgemeqni10Z_BOdA2U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP400482.RAdMmQarpK0b-ZTg-K_Vu4_XOVIfgemeqni10Z_BOdA2U130_provenance.