Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP736541.RAX8MkL-CoujmQFNkWRiroTCSJrH_wXs51GYdo9LDEC_o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP736541.RAX8MkL-CoujmQFNkWRiroTCSJrH_wXs51GYdo9LDEC_o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP736541.RAX8MkL-CoujmQFNkWRiroTCSJrH_wXs51GYdo9LDEC_o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP736541.RAX8MkL-CoujmQFNkWRiroTCSJrH_wXs51GYdo9LDEC_o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP736541.RAX8MkL-CoujmQFNkWRiroTCSJrH_wXs51GYdo9LDEC_o130_provenance.
- NP736541.RAX8MkL-CoujmQFNkWRiroTCSJrH_wXs51GYdo9LDEC_o130_assertion wasGeneratedBy ECO_0000203 NP736541.RAX8MkL-CoujmQFNkWRiroTCSJrH_wXs51GYdo9LDEC_o130_provenance.
- NP736541.RAX8MkL-CoujmQFNkWRiroTCSJrH_wXs51GYdo9LDEC_o130_assertion wasDerivedFrom befree-20150227 NP736541.RAX8MkL-CoujmQFNkWRiroTCSJrH_wXs51GYdo9LDEC_o130_provenance.
- NP736541.RAX8MkL-CoujmQFNkWRiroTCSJrH_wXs51GYdo9LDEC_o130_assertion SIO_000772 12482844 NP736541.RAX8MkL-CoujmQFNkWRiroTCSJrH_wXs51GYdo9LDEC_o130_provenance.
- NP736541.RAX8MkL-CoujmQFNkWRiroTCSJrH_wXs51GYdo9LDEC_o130_assertion evidence source_evidence_literature NP736541.RAX8MkL-CoujmQFNkWRiroTCSJrH_wXs51GYdo9LDEC_o130_provenance.
- NP736541.RAX8MkL-CoujmQFNkWRiroTCSJrH_wXs51GYdo9LDEC_o130_assertion description "[For the THBS-4 A387P polymorphism, additional studies are required to elucidate its role in premature CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP736541.RAX8MkL-CoujmQFNkWRiroTCSJrH_wXs51GYdo9LDEC_o130_provenance.