Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP485986.RAbfmAzn_3-DFCP4sBTVKQ16eAdJHTBSIV3gx8DeK0meo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP485986.RAbfmAzn_3-DFCP4sBTVKQ16eAdJHTBSIV3gx8DeK0meo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP485986.RAbfmAzn_3-DFCP4sBTVKQ16eAdJHTBSIV3gx8DeK0meo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP485986.RAbfmAzn_3-DFCP4sBTVKQ16eAdJHTBSIV3gx8DeK0meo130_provenance.
- NP485986.RAbfmAzn_3-DFCP4sBTVKQ16eAdJHTBSIV3gx8DeK0meo130_assertion description "[TSP-5 is of interest because mutations in the gene cause two skeletal dysplasias, pseudoachondroplasia (PSACH) and multiple epiphyseal dysplasia (MED/EDM1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP485986.RAbfmAzn_3-DFCP4sBTVKQ16eAdJHTBSIV3gx8DeK0meo130_provenance.
- NP485986.RAbfmAzn_3-DFCP4sBTVKQ16eAdJHTBSIV3gx8DeK0meo130_assertion evidence source_evidence_literature NP485986.RAbfmAzn_3-DFCP4sBTVKQ16eAdJHTBSIV3gx8DeK0meo130_provenance.
- NP485986.RAbfmAzn_3-DFCP4sBTVKQ16eAdJHTBSIV3gx8DeK0meo130_assertion SIO_000772 18193163 NP485986.RAbfmAzn_3-DFCP4sBTVKQ16eAdJHTBSIV3gx8DeK0meo130_provenance.
- NP485986.RAbfmAzn_3-DFCP4sBTVKQ16eAdJHTBSIV3gx8DeK0meo130_assertion wasDerivedFrom befree-20140225 NP485986.RAbfmAzn_3-DFCP4sBTVKQ16eAdJHTBSIV3gx8DeK0meo130_provenance.
- NP485986.RAbfmAzn_3-DFCP4sBTVKQ16eAdJHTBSIV3gx8DeK0meo130_assertion wasGeneratedBy ECO_0000203 NP485986.RAbfmAzn_3-DFCP4sBTVKQ16eAdJHTBSIV3gx8DeK0meo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP485986.RAbfmAzn_3-DFCP4sBTVKQ16eAdJHTBSIV3gx8DeK0meo130_provenance.