Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP670736.RAv_67Jy6v-pH2qcgOmUHNHIZw-7CM8q-j50pbpwwhGDY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP670736.RAv_67Jy6v-pH2qcgOmUHNHIZw-7CM8q-j50pbpwwhGDY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP670736.RAv_67Jy6v-pH2qcgOmUHNHIZw-7CM8q-j50pbpwwhGDY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP670736.RAv_67Jy6v-pH2qcgOmUHNHIZw-7CM8q-j50pbpwwhGDY130_provenance.
- NP670736.RAv_67Jy6v-pH2qcgOmUHNHIZw-7CM8q-j50pbpwwhGDY130_assertion description "[Mutations in the gene coding for the transmembrane receptor protein Patched (PTCH) are implicated in the autosomal dominant disorder Gorlin syndrome (also known as naevoid basal cell carcinoma syndrome), characterized by congenital abnormalities and cancer predisposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670736.RAv_67Jy6v-pH2qcgOmUHNHIZw-7CM8q-j50pbpwwhGDY130_provenance.
- NP670736.RAv_67Jy6v-pH2qcgOmUHNHIZw-7CM8q-j50pbpwwhGDY130_assertion evidence source_evidence_literature NP670736.RAv_67Jy6v-pH2qcgOmUHNHIZw-7CM8q-j50pbpwwhGDY130_provenance.
- NP670736.RAv_67Jy6v-pH2qcgOmUHNHIZw-7CM8q-j50pbpwwhGDY130_assertion SIO_000772 18476955 NP670736.RAv_67Jy6v-pH2qcgOmUHNHIZw-7CM8q-j50pbpwwhGDY130_provenance.
- NP670736.RAv_67Jy6v-pH2qcgOmUHNHIZw-7CM8q-j50pbpwwhGDY130_assertion wasDerivedFrom befree-2016 NP670736.RAv_67Jy6v-pH2qcgOmUHNHIZw-7CM8q-j50pbpwwhGDY130_provenance.
- NP670736.RAv_67Jy6v-pH2qcgOmUHNHIZw-7CM8q-j50pbpwwhGDY130_assertion wasGeneratedBy ECO_0000203 NP670736.RAv_67Jy6v-pH2qcgOmUHNHIZw-7CM8q-j50pbpwwhGDY130_provenance.
- befree-2016 importedOn "2016-02-19" NP670736.RAv_67Jy6v-pH2qcgOmUHNHIZw-7CM8q-j50pbpwwhGDY130_provenance.