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- source_evidence_literature type ECO_0000212 NP599756.RAwjkym_3xijr0KutlVc48zpwLgT_ximeB6WAUnmk6o1Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP599756.RAwjkym_3xijr0KutlVc48zpwLgT_ximeB6WAUnmk6o1Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP599756.RAwjkym_3xijr0KutlVc48zpwLgT_ximeB6WAUnmk6o1Q130_provenance.
- NP599756.RAwjkym_3xijr0KutlVc48zpwLgT_ximeB6WAUnmk6o1Q130_assertion description "[It seems likely that this technology will also have an impact on the management of sporadic MTC, although it is still too early to define a specific role for mutational analysis in these patients, except to exclude hereditary disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP599756.RAwjkym_3xijr0KutlVc48zpwLgT_ximeB6WAUnmk6o1Q130_provenance.
- NP599756.RAwjkym_3xijr0KutlVc48zpwLgT_ximeB6WAUnmk6o1Q130_assertion evidence source_evidence_literature NP599756.RAwjkym_3xijr0KutlVc48zpwLgT_ximeB6WAUnmk6o1Q130_provenance.
- NP599756.RAwjkym_3xijr0KutlVc48zpwLgT_ximeB6WAUnmk6o1Q130_assertion SIO_000772 7575334 NP599756.RAwjkym_3xijr0KutlVc48zpwLgT_ximeB6WAUnmk6o1Q130_provenance.
- NP599756.RAwjkym_3xijr0KutlVc48zpwLgT_ximeB6WAUnmk6o1Q130_assertion wasDerivedFrom befree-20150227 NP599756.RAwjkym_3xijr0KutlVc48zpwLgT_ximeB6WAUnmk6o1Q130_provenance.
- NP599756.RAwjkym_3xijr0KutlVc48zpwLgT_ximeB6WAUnmk6o1Q130_assertion wasGeneratedBy ECO_0000203 NP599756.RAwjkym_3xijr0KutlVc48zpwLgT_ximeB6WAUnmk6o1Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP599756.RAwjkym_3xijr0KutlVc48zpwLgT_ximeB6WAUnmk6o1Q130_provenance.