Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP412126.RAILAn_hJql-XuGKsVRpVBltXI4NUpzHDfzSk8hkzT4sA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP412126.RAILAn_hJql-XuGKsVRpVBltXI4NUpzHDfzSk8hkzT4sA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP412126.RAILAn_hJql-XuGKsVRpVBltXI4NUpzHDfzSk8hkzT4sA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP412126.RAILAn_hJql-XuGKsVRpVBltXI4NUpzHDfzSk8hkzT4sA130_provenance.
- NP412126.RAILAn_hJql-XuGKsVRpVBltXI4NUpzHDfzSk8hkzT4sA130_assertion description "[Our results strongly suggest that the clinical heterogeneity in XP-A is due to different mutations in the XPAC gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412126.RAILAn_hJql-XuGKsVRpVBltXI4NUpzHDfzSk8hkzT4sA130_provenance.
- NP412126.RAILAn_hJql-XuGKsVRpVBltXI4NUpzHDfzSk8hkzT4sA130_assertion evidence source_evidence_literature NP412126.RAILAn_hJql-XuGKsVRpVBltXI4NUpzHDfzSk8hkzT4sA130_provenance.
- NP412126.RAILAn_hJql-XuGKsVRpVBltXI4NUpzHDfzSk8hkzT4sA130_assertion SIO_000772 1372103 NP412126.RAILAn_hJql-XuGKsVRpVBltXI4NUpzHDfzSk8hkzT4sA130_provenance.
- NP412126.RAILAn_hJql-XuGKsVRpVBltXI4NUpzHDfzSk8hkzT4sA130_assertion wasDerivedFrom befree-2016 NP412126.RAILAn_hJql-XuGKsVRpVBltXI4NUpzHDfzSk8hkzT4sA130_provenance.
- NP412126.RAILAn_hJql-XuGKsVRpVBltXI4NUpzHDfzSk8hkzT4sA130_assertion wasGeneratedBy ECO_0000203 NP412126.RAILAn_hJql-XuGKsVRpVBltXI4NUpzHDfzSk8hkzT4sA130_provenance.
- befree-2016 importedOn "2016-02-19" NP412126.RAILAn_hJql-XuGKsVRpVBltXI4NUpzHDfzSk8hkzT4sA130_provenance.