Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294994.RA1xetU6Pi6kPRnofncKiqEx5j4-kgAx9LaEFV4GcCYEM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP294994.RA1xetU6Pi6kPRnofncKiqEx5j4-kgAx9LaEFV4GcCYEM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294994.RA1xetU6Pi6kPRnofncKiqEx5j4-kgAx9LaEFV4GcCYEM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294994.RA1xetU6Pi6kPRnofncKiqEx5j4-kgAx9LaEFV4GcCYEM130_provenance.
- NP294994.RA1xetU6Pi6kPRnofncKiqEx5j4-kgAx9LaEFV4GcCYEM130_assertion description "[In addition, he has vertebral anomalies, brachymelia of the arms, and a ventricular septal defect-features that are reminiscent of Robinow syndrome, which has also been shown to be caused by mutations in ROR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294994.RA1xetU6Pi6kPRnofncKiqEx5j4-kgAx9LaEFV4GcCYEM130_provenance.
- NP294994.RA1xetU6Pi6kPRnofncKiqEx5j4-kgAx9LaEFV4GcCYEM130_assertion evidence source_evidence_literature NP294994.RA1xetU6Pi6kPRnofncKiqEx5j4-kgAx9LaEFV4GcCYEM130_provenance.
- NP294994.RA1xetU6Pi6kPRnofncKiqEx5j4-kgAx9LaEFV4GcCYEM130_assertion SIO_000772 10986040 NP294994.RA1xetU6Pi6kPRnofncKiqEx5j4-kgAx9LaEFV4GcCYEM130_provenance.
- NP294994.RA1xetU6Pi6kPRnofncKiqEx5j4-kgAx9LaEFV4GcCYEM130_assertion wasDerivedFrom befree-2016 NP294994.RA1xetU6Pi6kPRnofncKiqEx5j4-kgAx9LaEFV4GcCYEM130_provenance.
- NP294994.RA1xetU6Pi6kPRnofncKiqEx5j4-kgAx9LaEFV4GcCYEM130_assertion wasGeneratedBy ECO_0000203 NP294994.RA1xetU6Pi6kPRnofncKiqEx5j4-kgAx9LaEFV4GcCYEM130_provenance.
- befree-2016 importedOn "2016-02-19" NP294994.RA1xetU6Pi6kPRnofncKiqEx5j4-kgAx9LaEFV4GcCYEM130_provenance.